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

页码：1710 / 1715

页数：6

共 37 条

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