Genetic inheritance of Gilbert's syndrome

Author:

Bosma PiterJ,Roy Chowdhury Jayanta,Jansen PeterH.M,Sato Hiroshi,Adachi Yukihiko,Aono Sachiko,Uyama Eiichiro,Nanno Tatsuo,Keino Hiroomi,Yamada Yasukazu,Koiwai Osamu

Publisher

Elsevier BV

Subject

General Medicine

Reference9 articles.

1. A mutation in bilirubin uridine 5'-diphosphate isoform I causing Crigler-Najjar type II;Bosma;Gastroenterology,1993

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

3. The novel bilirubin/phenol udp-glucuronosyltransferase ugtl gene locus: implications for multiple nonhemolytic familial hyperbilirubinemia;Owens;Pharmacogenetics,1992

4. Presence of an additional TA in the TATAA box of B-UGT1 correlates with Gilbert's syndrome;Bosma;Hepatology,1994

5. O. Koiwai, M. Nishizawa, K. Hasada, et al., Hum Mol Genet ((in press)).

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