Cytochromec oxidase: Organ-specific isoenzymes and deficiencies
Copyright policy )Cytochromec oxidase: Organ-specific isoenzymes and deficiencies
Ever since the first report of Luft et al. (1962), considerable information has become available on inherited metabolic diseases originating from defects in mitochondria. Apart from defects in the import of substrates, in the carboxylic acid cycle, and in fatty acid oxidation, many dysfunctions have been described in the mitochondrial respiratory chain and ATP synthase (Morgan-Hughes, 1980). In the present study, we focused on defects of cytochrome c oxidase (E.C. 1.9.3.1), the terminal component of the mitochondrial respiratory chain.
- Amsterdam UMC Netherlands
- University of Amsterdam Netherlands
Electron Transport Complex IV, Isoenzymes, Cytochrome-c Oxidase Deficiency, Humans, Mitochondria, Heart, Mitochondria, Muscle
Electron Transport Complex IV, Isoenzymes, Cytochrome-c Oxidase Deficiency, Humans, Mitochondria, Heart, Mitochondria, Muscle
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