Crigler-Najjar syndrome type II in a caucasian patient resulting from two mutations in the bilirubin uridine 5'-diphosphate-glucuronosyltransferase (UGT1A1) gene. - Suppr | 超能文献

Crigler-Najjar syndrome type II in a caucasian patient resulting from two mutations in the bilirubin uridine 5'-diphosphate-glucuronosyltransferase (UGT1A1) gene.

作者信息

Kraemer Doris, Klinker Hartwig

出版信息

J Hepatol. 2002 May;36(5):706-7. doi: 10.1016/s0168-8278(02)00034-x.

DOI:10.1016/s0168-8278(02)00034-x

Abstract

摘要

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