HUMAN DIHYDROXYACETONEPHOSPHATE ACYLTRANSFERASE DEFICIENCY - A NEW PEROXISOMAL DISORDER

被引：113

作者：

WANDERS, RJA

SCHUMACHER, H

HEIKOOP, J

SCHUTGENS, RBH

TAGER, JM

机构：

[1] KRANKENHAUS RENSCHEID LENNEP,REMSCHEID,GERMANY

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

来源：

JOURNAL OF INHERITED METABOLIC DISEASE | 1992年 / 15卷 / 03期

关键词：

D O I：

10.1007/BF02435984

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

[No abstract available]

引用

页码：389 / 391

页数：3

共 6 条

[1]

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[2]

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[3]

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[4] PEROXISOMAL ENZYME-ACTIVITIES IN THE HUMAN HEPATOBLASTOMA CELL LINE-HEPG2 AS COMPARED TO HUMAN LIVER [J].

WANDERS, RJA ;

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[5] PEROXISOMAL DISORDERS IN NEUROLOGY [J].

WANDERS, RJA ;

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SCHUTGENS, RBH ;

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TAGER, JM .

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[6] PEROXISOMAL VERY LONG-CHAIN FATTY-ACID BETA-OXIDATION IN HUMAN-SKIN FIBROBLASTS - ACTIVITY IN ZELLWEGER SYNDROME AND OTHER PEROXISOMAL DISORDERS [J].

WANDERS, RJA ;

VANROERMUND, CWT ;

VANWIJLAND, MJA ;

HEIKOOP, J ;

SCHUTGENS, RBH ;

SCHRAM, AW ;

TAGER, JM ;

VANDENBOSCH, H ;

POLLTHE, BT ;

SAUDUBRAY, JM ;

MOSER, HW ;

MOSER, AB .

CLINICA CHIMICA ACTA, 1987, 166 (2-3) :255-263

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