FAMILIAL MITOCHONDRIAL COMPLEX-I DEFICIENCY WITH AN ABNORMAL MITOCHONDRIAL ENCODED PROTEIN

被引：1

作者：

BARTH, PG

BOLHUIS, PA

WIJBURG, FA

SINJORGO, KMC

RUITENBEEK, W

SCHUTGENS, RBH

机构：

[1] UNIV AMSTERDAM HOSP,DEPT PEDIAT,AMSTERDAM,NETHERLANDS

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

[3] UNIV HOSP NIJMEGEN,DEPT PEDIAT,NIJMEGEN,NETHERLANDS

来源：

JOURNAL OF INHERITED METABOLIC DISEASE | 1989年 / 12卷

关键词：

D O I：

10.1007/BF03335421

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：355 / 357

页数：3

共 6 条

[1] HIGH-RESOLUTION ELECTROPHORETIC FRACTIONATION AND PARTIAL CHARACTERIZATION OF THE MITOCHONDRIAL TRANSLATION PRODUCTS FROM HELA-CELLS [J].

CHING, E ;

ATTARDI, G .

BIOCHEMISTRY, 1982, 21 (13) :3188-3195

[2] 6 UNIDENTIFIED READING FRAMES OF HUMAN MITOCHONDRIAL-DNA ENCODE COMPONENTS OF THE RESPIRATORY-CHAIN NADH DEHYDROGENASE [J].

CHOMYN, A ;

MARIOTTINI, P ;

CLEETER, MWJ ;

RAGAN, CI ;

MATSUNOYAGI, A ;

HATEFI, Y ;

DOOLITTLE, RF ;

ATTARDI, G .

NATURE, 1985, 314 (6012) :592-597

[3] MITOCHONDRIAL INHERITANCE IN A MITOCHONDRIALLY MEDIATED DISEASE [J].

EGGER, J ;

WILSON, J .

NEW ENGLAND JOURNAL OF MEDICINE, 1983, 309 (03) :142-146

[4] MITOCHONDRIAL-DNA AND GENETIC-DISEASE [J].

POULTON, J .

ARCHIVES OF DISEASE IN CHILDHOOD, 1988, 63 (08) :883-885

[5] MATERNALLY INHERITED MITOCHONDRIAL MYOPATHY AND MYOCLONIC EPILEPSY [J].

ROSING, HS ;

HOPKINS, LC ;

WALLACE, DC ;

EPSTEIN, CM ;

WEIDENHEIM, K .

ANNALS OF NEUROLOGY, 1985, 17 (03) :228-237

[6] FAMILIAL NADH - Q1 OXIDOREDUCTASE (COMPLEX-I) DEFICIENCY - VARIABLE EXPRESSION AND POSSIBLE TREATMENT [J].

WIJBURG, FA ;

BARTH, PG ;

RUITENBEEK, W ;

WANDERS, RJA ;

VOS, GD ;

VANAMSTEL, SLBP ;

SCHUTGENS, RBH .

JOURNAL OF INHERITED METABOLIC DISEASE, 1989, 12 :349-351

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