GENETIC INHERITANCE OF GILBERTS-SYNDROME

被引:36
作者
BOSMA, PJ
CHOWDHURY, JR
JANSEN, PHM
机构
来源
LANCET | 1995年 / 346卷 / 8970期
关键词
D O I
10.1016/S0140-6736(95)92203-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:314 / 315
页数:2
相关论文
共 5 条
[1]  
AONO, 1995, LANCET 0415, P958
[2]   A MUTATION IN BILIRUBIN URIDINE 5'-DIPHOSPHATE-GLUCURONOSYLTRANSFERASE ISOFORM-1 CAUSING CRIGLER-NAJJAR SYNDROME TYPE-II [J].
BOSMA, PJ ;
GOLDHOORN, B ;
ELFERINK, RPJO ;
SINAASAPPEL, M ;
OOSTRA, BA ;
JANSEN, PLM .
GASTROENTEROLOGY, 1993, 105 (01) :216-220
[3]  
BOSMA PJ, 1994, HEPATOLOGY, V20, P680
[4]  
BOSMA PJ, 1994, J BIOL CHEM, V179, P60
[5]   THE NOVEL BILIRUBIN PHENOL UDP-GLUCURONOSYLTRANSFERASE UGT1 GENE LOCUS - IMPLICATIONS FOR MULTIPLE NONHEMOLYTIC FAMILIAL HYPERBILIRUBINEMIA PHENOTYPES [J].
OWENS, IS ;
RITTER, JK .
PHARMACOGENETICS, 1992, 2 (03) :93-108