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

✍ Scribed by Kazuo Yamamoto; Hiroshi Sato; Yoshihide Fujiyama; Yukio Doida; Tadao Bamba

• Book ID: 117618299
• Publisher: Elsevier Science
• Year: 1998
• Tongue: English
• Weight: 210 KB
• Volume: 1406
• Category: Article
• ISSN: 0925-4439
• DOI: 10.1016/s0925-4439(98)00013-1