THE LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE OF HUMAN LIVER-MITOCHONDRIA

被引：9

作者：

CARPENTER, K ^{[1
]}

MIDDLETON, B ^{[1
]}

POLLITT, RJ ^{[1
]}

机构：

[1] SHEFFIELD UNIV,CHILDRENS HOSP,DEPT PAEDIAT,SHEFFIELD S10 2TH,ENGLAND

来源：

JOURNAL OF INHERITED METABOLIC DISEASE | 1991年 / 14卷 / 03期

关键词：

D O I：

10.1007/BF01811693

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

[No abstract available]

引用

收藏

页码：321 / 324

页数：4

相关论文

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[1] THE EXISTENCE OF AN INNER-MEMBRANE-BOUND, LONG ACYL-CHAIN-SPECIFIC 3-HYDROXYACYL-COA DEHYDROGENASE IN MAMMALIAN MITOCHONDRIA
ELFAKHRI, M
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[J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1982, 713 (02) : 270 - 279
[2] HALE DE, 1990, FATTY ACID OXIDATION, P503
[3] DISORDERS OF MITOCHONDRIAL BETA-OXIDATION - PRENATAL AND EARLY POSTNATAL DIAGNOSIS AND THEIR RELEVANCE TO REYES-SYNDROME AND SUDDEN INFANT DEATH
POLLITT, RJ
[J]. JOURNAL OF INHERITED METABOLIC DISEASE, 1989, 12 : 215 - 230
[4] POLLITT RJ, 1990, FATTY ACID OXIDATION, P495
[5] LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE-DEFICIENCY - IDENTIFICATION OF A NEW INBORN ERROR OF MITOCHONDRIAL FATTY-ACID BETA-OXIDATION
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[J]. JOURNAL OF INHERITED METABOLIC DISEASE, 1990, 13 (03) : 311 - 314