GENETIC-POLYMORPHISM OF HUMAN CYTOCHROME-P-450 (S)-MEPHENYTOIN 4-HYDROXYLASE - STUDIES WITH HUMAN AUTOANTIBODIES SUGGEST A FUNCTIONALLY ALTERED CYTOCHROME-P-450 ISOZYME AS CAUSE OF THE GENETIC DEFICIENCY

被引：48
作者：
MEIER, UT [1 ]
MEYER, UA [1 ]
机构：
[1] UNIV BASEL,BIOCTR,DEPT PHARMACOL,CH-4056 BASEL,SWITZERLAND
来源：
BIOCHEMISTRY | 1987年 / 26卷 / 25期
关键词：
D O I：
10.1021/bi00399a065
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
引用
收藏
页码：8466 / 8474
页数：9
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