Contribution of two missense mutations (G71R and Y486D) of the bilirubin UDP glycosyltransferase (UGT1A1) gene to phenotypes of Gilbert's syndrome and Crigler–Najjar syndrome type II-Reference-Cited by-同舟云学术

Contribution of two missense mutations (G71R and Y486D) of the bilirubin UDP glycosyltransferase (UGT1A1) gene to phenotypes of Gilbert's syndrome and Crigler–Najjar syndrome type II

Published:1998-04 Issue:3 Volume:1406 Page:267-273
ISSN:0925-4439
Container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
language:en
Short-container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Author:

Yamamoto Kazuo,Sato Hiroshi,Fujiyama Yoshihide,Doida Yukio,Bamba Tadao

Publisher

Elsevier BV

Subject

Molecular Biology,Molecular Medicine

Reference28 articles.

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4. Hepatic bilirubin UDP-glucuronyl transferase activity in liver disease and Gilbert's syndrome;Black;New Engl. J. Med.,1969

5. Hepatic bilirubin-conjugating enzymes of man in the normal state and in liver disease;Adachi;Gastroenterol. Jpn.,1982

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