Mitochondrial myopathy: tissue-specific expression of a defect in ubiquinol-cytochrome c reductase-Reference-Cited by-同舟云学术

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Mitochondrial myopathy: tissue-specific expression of a defect in ubiquinol-cytochrome c reductase

Published:1986-08 Issue:3 Volume:158 Page:253-261
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

Darley-Usmar Victor M.,Watanabe Masahiko,Uchiyama Yasuo,Kondo Ikuko,Kennaway Nancy G.,Gronke Lisa,Hamaguchi Hideo

Publisher

Elsevier BV

Subject

Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine

Reference22 articles.

1. Fatal infantile mitochondrial myopathy and renal dysfunction due to cytochrome-c-oxidase deficiency;DiMauro;Neurology,1980

2. A mitochondrial myopathy characterized by a deficiency in reducible cytochrome b;Morgan-Hughes;Brain,1977

3. Mitochondrial encephalomyopathies. Biochemical studies in two cases revealing defects in the respiratory chain;Morgan-Hughes;Brain,1982

4. Mitochondrial myopathies: defects in mitochondrial metabolism in human skeletal muscle;Clark;Biochem Soc Trans,1983

5. Histiocytoid cardiomyopathy of infancy: deficiency of reducible cytochrome b in heart mitochondria;Papadimitriou;Pediatr Res,1984

Cited by 21 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Metabolic Myopathies;Swaiman's Pediatric Neurology;2012

2. Antibody-based approaches to diagnosis and characterization of oxidative phosphorylation diseases;Mitochondrion;2001-10

3. Mitochondrial Encephalomyopathy and Complex III Deficiency Associated with a Stop-Codon Mutation in the Cytochrome b Gene;The American Journal of Human Genetics;2000-12

4. Utility of multimodal evoked potential study and electroencephalography in mitochondrial encephalomyopathy;The Italian Journal of Neurological Sciences;1998-10

5. Clinical heterogeneity in respiratory chain complex III deficiency in childhood;Journal of the Neurological Sciences;1997-07

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