Crigler-Najjar syndrome type II in a caucasian patient resulting from two mutations in the bilirubin uridine 5'-diphosphate-glucuronosyltransferase (UGT1A1) gene.
Crigler-Najjar syndrome type II in a caucasian patient resulting from two mutations in the bilirubin uridine 5'-diphosphate-glucuronosyltransferase (UGT1A1) gene.
复制标题
一名白种人患者患有 II 型克里格勒-纳贾尔综合征，由胆红素尿苷 5-二磷酸-葡萄糖醛酸基转移酶 (UGT1A1) 基因的两次突变引起。
作者：
D. Kraemer;H. Klinker
