X-LINKED ADRENOLEUKODYSTROPHY - IDENTIFICATION OF THE PRIMARY DEFECT AT THE LEVEL OF A DEFICIENT PEROXISOMAL VERY LONG-CHAIN FATTY ACYL-COA SYNTHETASE USING A NEWLY DEVELOPED METHOD FOR THE ISOLATION OF PEROXISOMES FROM SKIN FIBROBLASTS

被引：28

作者：

WANDERS, RJA

VANROERMUND, CWT

VANWIJLAND, MJA

SCHUTGENS, RBH

SCHRAM, AW

TAGER, JM

VANDENBOSCH, H

SCHALKWIJK, C

机构：

[1] STATE UNIV UTRECHT,BIOCHEM LAB,3584 CH UTRECHT,NETHERLANDS

[2] UNIV AMSTERDAM,DEPT BIOCHEM,1105 AZ AMSTERDAM,NETHERLANDS

来源：

JOURNAL OF INHERITED METABOLIC DISEASE | 1988年 / 11卷

关键词：

D O I：

10.1007/BF01804228

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：173 / 177

页数：5

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