Hematologically important mutations: Bilirubin UDP-glucuronosyltransferase gene mutations in Gilbert and Crigler–Najjar syndromes
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Hematology,Molecular Biology,Molecular Medicine
Reference35 articles.
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3. Wintrobe's Clinical Haematology;Lee,1993
4. Nathan and Oski's Haematology of Infancy and Childhood;Nathan,1998
5. Sequence of exons and the flanking regions of human bilirubin–UDP-glucuronosyltransferase gene complex and identification of a genetic mutation in a patient with Crigler–Najjar syndrome type I;Bosma;Hepatology,1992
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