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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

Author:

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

Publication:

Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Publisher:

Elsevier

Date:

28 April 1998

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