GENETIC-HETEROGENEITY IN THE CEREBROHEPATORENAL (ZELLWEGER) SYNDROME AND OTHER INHERITED DISORDERS WITH A GENERALIZED IMPAIRMENT OF PEROXISOMAL FUNCTIONS - A STUDY USING COMPLEMENTATION ANALYSIS

被引：135
|
作者：
BRUL, S
WESTERVELD, A
STRIJLAND, A
WANDERS, RJA
SCHRAM, AW
HEYMANS, HSA
SCHUTGENS, RBH
VANDENBOSCH, H
TAGER, JM
机构：
[1] UNIV AMSTERDAM,BIOCHEM LAB,1105 AZ AMSTERDAM,NETHERLANDS
[2] ERASMUS UNIV,DIV CELL BIOL & GENET,3000 DR ROTTERDAM,NETHERLANDS
[3] UNIV AMSTERDAM HOSP,DEPT PEDIAT,1105 AZ AMSTERDAM,NETHERLANDS
[4] STATE UNIV UTRECHT,BIOCHEM LAB,3584 CH UTRECHT,NETHERLANDS
来源：
JOURNAL OF CLINICAL INVESTIGATION | 1988年 / 81卷 / 06期
关键词：
D O I：
10.1172/JCI113510
中图分类号：
R-3 [医学研究方法]; R3 [基础医学];
学科分类号：
1001 ;
摘要：
引用
收藏
页码：1710 / 1715
页数：6
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