The Effect of UGT1A1 Promoter Polymorphism in the Development of Hyperbilirubinemia and Cholelithiasis in Hemoglobinopathy Patients

Author:

AlFadhli Suad,Al-Jafer Hassan,Hadi Mays,Al-Mutairi Mashael,Nizam Rasheeba

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference41 articles.

1. Bilirubin UDP-glucuronosyltransferase 1 is the only relevant bilirubin glucuronidating isoform in man;PJ Bosma;J Biol Chem,1994

2. Hepatobiliary system in sickle cell disease;TT Schubert;Gastroenterology,1987

3. Molecular pathology of Crigler–Najjar type I and II and Gilbert’s syndromes;M Sampietro;Haematologica,1999

4. Inherited disorders of bilirubin metabolism;PJ Bosma;J Hepatol,2003

5. Genetic defects of the UDP-glucuronosyltransferase-1 (UGT1) gene that cause familial non-haemolytic unconjugated hyperbilirubinaemias;DJ Clarke;Clin Chim Acta,1997

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