Gilbert's Syndrome Hemolytic Anemia . Gilbert syndrome is an autosomal recessive disorder of bilirubin metabolism within the liver. Gilbert syndrome is a benign condition due to ugt1a1 mutations frequently resulting in mild, indirect. Reduced glucuronidation of bilirubin leads to. Gilbert syndrome is the most common inherited disorder of bilirubin glucuronidation. Gilbert’s syndrome manifests as mild unconjugated asymptomatic hyperbilirubinaemia, usually found in young adults during routine. Gilbert syndrome is an inherited disease characterised by mild unconjugated hyperbilirubinaemia caused by mutations in. Gilbert's syndrome (gs) is associated with a mild chronic unconjugated hyperbilirubinemia, due to. Warm autoimmune hemolytic anemia (waiha) is characterized by evidence of red blood cell (rbc) hemolysis and a direct.
from www.thebloodproject.com
Gilbert syndrome is the most common inherited disorder of bilirubin glucuronidation. Gilbert’s syndrome manifests as mild unconjugated asymptomatic hyperbilirubinaemia, usually found in young adults during routine. Gilbert syndrome is an inherited disease characterised by mild unconjugated hyperbilirubinaemia caused by mutations in. Reduced glucuronidation of bilirubin leads to. Warm autoimmune hemolytic anemia (waiha) is characterized by evidence of red blood cell (rbc) hemolysis and a direct. Gilbert's syndrome (gs) is associated with a mild chronic unconjugated hyperbilirubinemia, due to. Gilbert syndrome is a benign condition due to ugt1a1 mutations frequently resulting in mild, indirect. Gilbert syndrome is an autosomal recessive disorder of bilirubin metabolism within the liver.
Warm Autoimmune Hemolytic Anemia • The Blood Project
Gilbert's Syndrome Hemolytic Anemia Warm autoimmune hemolytic anemia (waiha) is characterized by evidence of red blood cell (rbc) hemolysis and a direct. Gilbert’s syndrome manifests as mild unconjugated asymptomatic hyperbilirubinaemia, usually found in young adults during routine. Warm autoimmune hemolytic anemia (waiha) is characterized by evidence of red blood cell (rbc) hemolysis and a direct. Gilbert syndrome is an autosomal recessive disorder of bilirubin metabolism within the liver. Gilbert syndrome is a benign condition due to ugt1a1 mutations frequently resulting in mild, indirect. Gilbert syndrome is the most common inherited disorder of bilirubin glucuronidation. Reduced glucuronidation of bilirubin leads to. Gilbert's syndrome (gs) is associated with a mild chronic unconjugated hyperbilirubinemia, due to. Gilbert syndrome is an inherited disease characterised by mild unconjugated hyperbilirubinaemia caused by mutations in.
From ilovepathology.com
Pathology of G6PD deficiency Pathology Made Simple Gilbert's Syndrome Hemolytic Anemia Warm autoimmune hemolytic anemia (waiha) is characterized by evidence of red blood cell (rbc) hemolysis and a direct. Gilbert syndrome is a benign condition due to ugt1a1 mutations frequently resulting in mild, indirect. Gilbert's syndrome (gs) is associated with a mild chronic unconjugated hyperbilirubinemia, due to. Reduced glucuronidation of bilirubin leads to. Gilbert syndrome is an autosomal recessive disorder of. Gilbert's Syndrome Hemolytic Anemia.
From www.labpedia.net
Gilbert’s Syndrome part 1 Gilbert's Syndrome Hemolytic Anemia Gilbert's syndrome (gs) is associated with a mild chronic unconjugated hyperbilirubinemia, due to. Gilbert syndrome is an autosomal recessive disorder of bilirubin metabolism within the liver. Gilbert syndrome is an inherited disease characterised by mild unconjugated hyperbilirubinaemia caused by mutations in. Gilbert’s syndrome manifests as mild unconjugated asymptomatic hyperbilirubinaemia, usually found in young adults during routine. Gilbert syndrome is a. Gilbert's Syndrome Hemolytic Anemia.
From www.slideshare.net
Acquired hemolytic anemia Gilbert's Syndrome Hemolytic Anemia Gilbert syndrome is the most common inherited disorder of bilirubin glucuronidation. Gilbert's syndrome (gs) is associated with a mild chronic unconjugated hyperbilirubinemia, due to. Reduced glucuronidation of bilirubin leads to. Gilbert’s syndrome manifests as mild unconjugated asymptomatic hyperbilirubinaemia, usually found in young adults during routine. Warm autoimmune hemolytic anemia (waiha) is characterized by evidence of red blood cell (rbc) hemolysis. Gilbert's Syndrome Hemolytic Anemia.
From www.slideserve.com
PPT Autoimmune Hemolytic Anemias PowerPoint Presentation, free Gilbert's Syndrome Hemolytic Anemia Reduced glucuronidation of bilirubin leads to. Gilbert syndrome is a benign condition due to ugt1a1 mutations frequently resulting in mild, indirect. Gilbert syndrome is an inherited disease characterised by mild unconjugated hyperbilirubinaemia caused by mutations in. Warm autoimmune hemolytic anemia (waiha) is characterized by evidence of red blood cell (rbc) hemolysis and a direct. Gilbert syndrome is an autosomal recessive. Gilbert's Syndrome Hemolytic Anemia.
From www.researchgate.net
(PDF) Gilbert syndrome in patients with inherited hemolytic anemia Gilbert's Syndrome Hemolytic Anemia Gilbert syndrome is an inherited disease characterised by mild unconjugated hyperbilirubinaemia caused by mutations in. Warm autoimmune hemolytic anemia (waiha) is characterized by evidence of red blood cell (rbc) hemolysis and a direct. Gilbert syndrome is a benign condition due to ugt1a1 mutations frequently resulting in mild, indirect. Gilbert’s syndrome manifests as mild unconjugated asymptomatic hyperbilirubinaemia, usually found in young. Gilbert's Syndrome Hemolytic Anemia.
From www.thebloodproject.com
Warm Autoimmune Hemolytic Anemia • The Blood Project Gilbert's Syndrome Hemolytic Anemia Gilbert syndrome is a benign condition due to ugt1a1 mutations frequently resulting in mild, indirect. Gilbert syndrome is an autosomal recessive disorder of bilirubin metabolism within the liver. Gilbert syndrome is the most common inherited disorder of bilirubin glucuronidation. Gilbert syndrome is an inherited disease characterised by mild unconjugated hyperbilirubinaemia caused by mutations in. Gilbert's syndrome (gs) is associated with. Gilbert's Syndrome Hemolytic Anemia.
From healthjade.com
Gilbert Syndrome Causes, Diagnosis, Complications, Treatment Gilbert's Syndrome Hemolytic Anemia Gilbert syndrome is an autosomal recessive disorder of bilirubin metabolism within the liver. Gilbert syndrome is the most common inherited disorder of bilirubin glucuronidation. Gilbert's syndrome (gs) is associated with a mild chronic unconjugated hyperbilirubinemia, due to. Gilbert syndrome is a benign condition due to ugt1a1 mutations frequently resulting in mild, indirect. Warm autoimmune hemolytic anemia (waiha) is characterized by. Gilbert's Syndrome Hemolytic Anemia.
From www.youtube.com
Hemolytic Anemia YouTube Gilbert's Syndrome Hemolytic Anemia Gilbert’s syndrome manifests as mild unconjugated asymptomatic hyperbilirubinaemia, usually found in young adults during routine. Gilbert's syndrome (gs) is associated with a mild chronic unconjugated hyperbilirubinemia, due to. Gilbert syndrome is an autosomal recessive disorder of bilirubin metabolism within the liver. Gilbert syndrome is a benign condition due to ugt1a1 mutations frequently resulting in mild, indirect. Gilbert syndrome is the. Gilbert's Syndrome Hemolytic Anemia.
From www.slideserve.com
PPT Hemolytic Anemias PowerPoint Presentation, free download ID588700 Gilbert's Syndrome Hemolytic Anemia Gilbert syndrome is an autosomal recessive disorder of bilirubin metabolism within the liver. Reduced glucuronidation of bilirubin leads to. Gilbert syndrome is the most common inherited disorder of bilirubin glucuronidation. Gilbert's syndrome (gs) is associated with a mild chronic unconjugated hyperbilirubinemia, due to. Gilbert’s syndrome manifests as mild unconjugated asymptomatic hyperbilirubinaemia, usually found in young adults during routine. Gilbert syndrome. Gilbert's Syndrome Hemolytic Anemia.
From chennailiverfoundation.org
All You Need To Know About Gilbert Syndrome Chennai Liver Foundation Gilbert's Syndrome Hemolytic Anemia Warm autoimmune hemolytic anemia (waiha) is characterized by evidence of red blood cell (rbc) hemolysis and a direct. Gilbert’s syndrome manifests as mild unconjugated asymptomatic hyperbilirubinaemia, usually found in young adults during routine. Gilbert's syndrome (gs) is associated with a mild chronic unconjugated hyperbilirubinemia, due to. Gilbert syndrome is an inherited disease characterised by mild unconjugated hyperbilirubinaemia caused by mutations. Gilbert's Syndrome Hemolytic Anemia.
From www.researchgate.net
(PDF) A Case of Congenital Hemolytic Anemia of Unknown Cause Combined Gilbert's Syndrome Hemolytic Anemia Gilbert syndrome is a benign condition due to ugt1a1 mutations frequently resulting in mild, indirect. Gilbert’s syndrome manifests as mild unconjugated asymptomatic hyperbilirubinaemia, usually found in young adults during routine. Gilbert's syndrome (gs) is associated with a mild chronic unconjugated hyperbilirubinemia, due to. Gilbert syndrome is an autosomal recessive disorder of bilirubin metabolism within the liver. Gilbert syndrome is the. Gilbert's Syndrome Hemolytic Anemia.
From www.labpedia.net
Gilbert’s Syndrome Diagnosis Part 2 Gilbert's Syndrome Hemolytic Anemia Gilbert syndrome is a benign condition due to ugt1a1 mutations frequently resulting in mild, indirect. Gilbert's syndrome (gs) is associated with a mild chronic unconjugated hyperbilirubinemia, due to. Gilbert syndrome is the most common inherited disorder of bilirubin glucuronidation. Gilbert’s syndrome manifests as mild unconjugated asymptomatic hyperbilirubinaemia, usually found in young adults during routine. Gilbert syndrome is an inherited disease. Gilbert's Syndrome Hemolytic Anemia.
From labpedia.net
Gilbert's Syndrome, Signs/Symptoms and Diagnosis Gilbert's Syndrome Hemolytic Anemia Gilbert syndrome is an inherited disease characterised by mild unconjugated hyperbilirubinaemia caused by mutations in. Warm autoimmune hemolytic anemia (waiha) is characterized by evidence of red blood cell (rbc) hemolysis and a direct. Gilbert's syndrome (gs) is associated with a mild chronic unconjugated hyperbilirubinemia, due to. Reduced glucuronidation of bilirubin leads to. Gilbert syndrome is a benign condition due to. Gilbert's Syndrome Hemolytic Anemia.
From www.aafp.org
Hemolytic Anemia Evaluation and Differential Diagnosis AAFP Gilbert's Syndrome Hemolytic Anemia Gilbert syndrome is an autosomal recessive disorder of bilirubin metabolism within the liver. Gilbert syndrome is an inherited disease characterised by mild unconjugated hyperbilirubinaemia caused by mutations in. Gilbert syndrome is a benign condition due to ugt1a1 mutations frequently resulting in mild, indirect. Gilbert’s syndrome manifests as mild unconjugated asymptomatic hyperbilirubinaemia, usually found in young adults during routine. Reduced glucuronidation. Gilbert's Syndrome Hemolytic Anemia.
From www.medindia.net
Hemolytic Anemia Causes, Symptoms, Diagnosis, Treatment Gilbert's Syndrome Hemolytic Anemia Warm autoimmune hemolytic anemia (waiha) is characterized by evidence of red blood cell (rbc) hemolysis and a direct. Gilbert syndrome is a benign condition due to ugt1a1 mutations frequently resulting in mild, indirect. Gilbert's syndrome (gs) is associated with a mild chronic unconjugated hyperbilirubinemia, due to. Gilbert syndrome is an inherited disease characterised by mild unconjugated hyperbilirubinaemia caused by mutations. Gilbert's Syndrome Hemolytic Anemia.
From a2zhealthy.com
Gilbert's Syndrome GS; Causes, Symptoms, Diagnosis & Treatment Gilbert's Syndrome Hemolytic Anemia Reduced glucuronidation of bilirubin leads to. Gilbert syndrome is an autosomal recessive disorder of bilirubin metabolism within the liver. Gilbert syndrome is an inherited disease characterised by mild unconjugated hyperbilirubinaemia caused by mutations in. Gilbert's syndrome (gs) is associated with a mild chronic unconjugated hyperbilirubinemia, due to. Gilbert’s syndrome manifests as mild unconjugated asymptomatic hyperbilirubinaemia, usually found in young adults. Gilbert's Syndrome Hemolytic Anemia.
From www.slideserve.com
PPT Haem13 hemolytic anemia acquired PowerPoint Presentation, free Gilbert's Syndrome Hemolytic Anemia Gilbert syndrome is a benign condition due to ugt1a1 mutations frequently resulting in mild, indirect. Gilbert’s syndrome manifests as mild unconjugated asymptomatic hyperbilirubinaemia, usually found in young adults during routine. Warm autoimmune hemolytic anemia (waiha) is characterized by evidence of red blood cell (rbc) hemolysis and a direct. Gilbert syndrome is an inherited disease characterised by mild unconjugated hyperbilirubinaemia caused. Gilbert's Syndrome Hemolytic Anemia.
From www.slideserve.com
PPT Haem14 Hemolytic anemia Congenital PowerPoint Presentation, free Gilbert's Syndrome Hemolytic Anemia Gilbert syndrome is an autosomal recessive disorder of bilirubin metabolism within the liver. Gilbert’s syndrome manifests as mild unconjugated asymptomatic hyperbilirubinaemia, usually found in young adults during routine. Gilbert syndrome is an inherited disease characterised by mild unconjugated hyperbilirubinaemia caused by mutations in. Reduced glucuronidation of bilirubin leads to. Warm autoimmune hemolytic anemia (waiha) is characterized by evidence of red. Gilbert's Syndrome Hemolytic Anemia.
From mavink.com
Hemolytic Anemia Blood Smear Gilbert's Syndrome Hemolytic Anemia Warm autoimmune hemolytic anemia (waiha) is characterized by evidence of red blood cell (rbc) hemolysis and a direct. Gilbert syndrome is an inherited disease characterised by mild unconjugated hyperbilirubinaemia caused by mutations in. Gilbert’s syndrome manifests as mild unconjugated asymptomatic hyperbilirubinaemia, usually found in young adults during routine. Reduced glucuronidation of bilirubin leads to. Gilbert syndrome is the most common. Gilbert's Syndrome Hemolytic Anemia.
From www.pinterest.com
View in full resolution Med School, Nursing School, Gilbert's Syndrome Gilbert's Syndrome Hemolytic Anemia Gilbert syndrome is the most common inherited disorder of bilirubin glucuronidation. Warm autoimmune hemolytic anemia (waiha) is characterized by evidence of red blood cell (rbc) hemolysis and a direct. Gilbert syndrome is an autosomal recessive disorder of bilirubin metabolism within the liver. Gilbert's syndrome (gs) is associated with a mild chronic unconjugated hyperbilirubinemia, due to. Gilbert syndrome is an inherited. Gilbert's Syndrome Hemolytic Anemia.
From labpedia.net
Gilbert's Syndrome, Signs/Symptoms and Diagnosis Gilbert's Syndrome Hemolytic Anemia Gilbert syndrome is the most common inherited disorder of bilirubin glucuronidation. Gilbert’s syndrome manifests as mild unconjugated asymptomatic hyperbilirubinaemia, usually found in young adults during routine. Warm autoimmune hemolytic anemia (waiha) is characterized by evidence of red blood cell (rbc) hemolysis and a direct. Reduced glucuronidation of bilirubin leads to. Gilbert syndrome is an inherited disease characterised by mild unconjugated. Gilbert's Syndrome Hemolytic Anemia.
From www.slideserve.com
PPT Hemolytic Anemias PowerPoint Presentation, free download ID4632555 Gilbert's Syndrome Hemolytic Anemia Warm autoimmune hemolytic anemia (waiha) is characterized by evidence of red blood cell (rbc) hemolysis and a direct. Gilbert syndrome is an autosomal recessive disorder of bilirubin metabolism within the liver. Gilbert syndrome is the most common inherited disorder of bilirubin glucuronidation. Gilbert’s syndrome manifests as mild unconjugated asymptomatic hyperbilirubinaemia, usually found in young adults during routine. Gilbert's syndrome (gs). Gilbert's Syndrome Hemolytic Anemia.
From www.slideserve.com
PPT Haem13 hemolytic anemia acquired PowerPoint Presentation, free Gilbert's Syndrome Hemolytic Anemia Reduced glucuronidation of bilirubin leads to. Gilbert syndrome is an inherited disease characterised by mild unconjugated hyperbilirubinaemia caused by mutations in. Gilbert's syndrome (gs) is associated with a mild chronic unconjugated hyperbilirubinemia, due to. Gilbert syndrome is an autosomal recessive disorder of bilirubin metabolism within the liver. Gilbert syndrome is the most common inherited disorder of bilirubin glucuronidation. Gilbert syndrome. Gilbert's Syndrome Hemolytic Anemia.
From inspiredmeded.com
How do you workup hemolytic anemia? Inspired MedEd Gilbert's Syndrome Hemolytic Anemia Gilbert syndrome is a benign condition due to ugt1a1 mutations frequently resulting in mild, indirect. Gilbert's syndrome (gs) is associated with a mild chronic unconjugated hyperbilirubinemia, due to. Gilbert’s syndrome manifests as mild unconjugated asymptomatic hyperbilirubinaemia, usually found in young adults during routine. Gilbert syndrome is an autosomal recessive disorder of bilirubin metabolism within the liver. Gilbert syndrome is the. Gilbert's Syndrome Hemolytic Anemia.
From www.slideserve.com
PPT Anemia PowerPoint Presentation, free download ID5701423 Gilbert's Syndrome Hemolytic Anemia Gilbert’s syndrome manifests as mild unconjugated asymptomatic hyperbilirubinaemia, usually found in young adults during routine. Gilbert syndrome is the most common inherited disorder of bilirubin glucuronidation. Gilbert syndrome is an inherited disease characterised by mild unconjugated hyperbilirubinaemia caused by mutations in. Gilbert syndrome is a benign condition due to ugt1a1 mutations frequently resulting in mild, indirect. Reduced glucuronidation of bilirubin. Gilbert's Syndrome Hemolytic Anemia.
From step2.medbullets.com
Autoimmune Hemolysis Heme Medbullets Step 2/3 Gilbert's Syndrome Hemolytic Anemia Warm autoimmune hemolytic anemia (waiha) is characterized by evidence of red blood cell (rbc) hemolysis and a direct. Gilbert's syndrome (gs) is associated with a mild chronic unconjugated hyperbilirubinemia, due to. Gilbert syndrome is an autosomal recessive disorder of bilirubin metabolism within the liver. Reduced glucuronidation of bilirubin leads to. Gilbert syndrome is a benign condition due to ugt1a1 mutations. Gilbert's Syndrome Hemolytic Anemia.
From studylib.net
Physiologic Classification of Anemia Hemolytic Anemias Gilbert's Syndrome Hemolytic Anemia Gilbert's syndrome (gs) is associated with a mild chronic unconjugated hyperbilirubinemia, due to. Gilbert syndrome is an autosomal recessive disorder of bilirubin metabolism within the liver. Warm autoimmune hemolytic anemia (waiha) is characterized by evidence of red blood cell (rbc) hemolysis and a direct. Gilbert syndrome is the most common inherited disorder of bilirubin glucuronidation. Gilbert syndrome is an inherited. Gilbert's Syndrome Hemolytic Anemia.
From slideplayer.com
THE MAIN HAEMATOLOGICAL SYNDROMES ppt download Gilbert's Syndrome Hemolytic Anemia Gilbert syndrome is an autosomal recessive disorder of bilirubin metabolism within the liver. Gilbert syndrome is a benign condition due to ugt1a1 mutations frequently resulting in mild, indirect. Gilbert's syndrome (gs) is associated with a mild chronic unconjugated hyperbilirubinemia, due to. Reduced glucuronidation of bilirubin leads to. Gilbert syndrome is the most common inherited disorder of bilirubin glucuronidation. Warm autoimmune. Gilbert's Syndrome Hemolytic Anemia.
From www.youtube.com
Hemolytic Anemias Part 4 G6PD Deficiency; Pathophysiology,Morphology Gilbert's Syndrome Hemolytic Anemia Gilbert syndrome is an autosomal recessive disorder of bilirubin metabolism within the liver. Gilbert syndrome is the most common inherited disorder of bilirubin glucuronidation. Gilbert syndrome is a benign condition due to ugt1a1 mutations frequently resulting in mild, indirect. Gilbert syndrome is an inherited disease characterised by mild unconjugated hyperbilirubinaemia caused by mutations in. Reduced glucuronidation of bilirubin leads to.. Gilbert's Syndrome Hemolytic Anemia.
From www.imreference.com
Hemolytic Anemia IM Reference Gilbert's Syndrome Hemolytic Anemia Warm autoimmune hemolytic anemia (waiha) is characterized by evidence of red blood cell (rbc) hemolysis and a direct. Gilbert syndrome is the most common inherited disorder of bilirubin glucuronidation. Gilbert syndrome is a benign condition due to ugt1a1 mutations frequently resulting in mild, indirect. Gilbert's syndrome (gs) is associated with a mild chronic unconjugated hyperbilirubinemia, due to. Gilbert syndrome is. Gilbert's Syndrome Hemolytic Anemia.
From www.dreamstime.com
Hemolytic Anemia stock vector. Illustration of immune 42917510 Gilbert's Syndrome Hemolytic Anemia Gilbert's syndrome (gs) is associated with a mild chronic unconjugated hyperbilirubinemia, due to. Gilbert’s syndrome manifests as mild unconjugated asymptomatic hyperbilirubinaemia, usually found in young adults during routine. Gilbert syndrome is the most common inherited disorder of bilirubin glucuronidation. Gilbert syndrome is an autosomal recessive disorder of bilirubin metabolism within the liver. Gilbert syndrome is a benign condition due to. Gilbert's Syndrome Hemolytic Anemia.
From www.slideserve.com
PPT Hemolysis PowerPoint Presentation, free download ID3517093 Gilbert's Syndrome Hemolytic Anemia Warm autoimmune hemolytic anemia (waiha) is characterized by evidence of red blood cell (rbc) hemolysis and a direct. Gilbert syndrome is an inherited disease characterised by mild unconjugated hyperbilirubinaemia caused by mutations in. Reduced glucuronidation of bilirubin leads to. Gilbert syndrome is the most common inherited disorder of bilirubin glucuronidation. Gilbert syndrome is an autosomal recessive disorder of bilirubin metabolism. Gilbert's Syndrome Hemolytic Anemia.
From www.slideserve.com
PPT Haem14 Hemolytic anemia Congenital PowerPoint Presentation, free Gilbert's Syndrome Hemolytic Anemia Gilbert syndrome is the most common inherited disorder of bilirubin glucuronidation. Gilbert syndrome is a benign condition due to ugt1a1 mutations frequently resulting in mild, indirect. Gilbert's syndrome (gs) is associated with a mild chronic unconjugated hyperbilirubinemia, due to. Gilbert syndrome is an inherited disease characterised by mild unconjugated hyperbilirubinaemia caused by mutations in. Reduced glucuronidation of bilirubin leads to.. Gilbert's Syndrome Hemolytic Anemia.
From mavink.com
Hemolytic Anemia Peripheral Smear Gilbert's Syndrome Hemolytic Anemia Reduced glucuronidation of bilirubin leads to. Warm autoimmune hemolytic anemia (waiha) is characterized by evidence of red blood cell (rbc) hemolysis and a direct. Gilbert’s syndrome manifests as mild unconjugated asymptomatic hyperbilirubinaemia, usually found in young adults during routine. Gilbert syndrome is an inherited disease characterised by mild unconjugated hyperbilirubinaemia caused by mutations in. Gilbert syndrome is an autosomal recessive. Gilbert's Syndrome Hemolytic Anemia.
From www.semanticscholar.org
Figure 1 from A Case of Congenital Hemolytic Anemia of Unknown Cause Gilbert's Syndrome Hemolytic Anemia Gilbert's syndrome (gs) is associated with a mild chronic unconjugated hyperbilirubinemia, due to. Gilbert syndrome is an inherited disease characterised by mild unconjugated hyperbilirubinaemia caused by mutations in. Gilbert syndrome is the most common inherited disorder of bilirubin glucuronidation. Reduced glucuronidation of bilirubin leads to. Gilbert syndrome is a benign condition due to ugt1a1 mutations frequently resulting in mild, indirect.. Gilbert's Syndrome Hemolytic Anemia.
