Defects in oxidative phosphorylation. Biochemical investigations in skeletal muscle and expression of the lesion in other cells. [electronic resource]
Producer: 19880113Description: 81-97 p. digitalISSN:- 0141-8955
- Adolescent
- Adult
- Biotin -- metabolism
- Brain -- enzymology
- Carnitine -- metabolism
- Cells, Cultured
- Child, Preschool
- Coenzyme A -- metabolism
- Cytochrome-c Oxidase Deficiency
- Electron Transport Complex III -- deficiency
- Female
- Fibroblasts -- enzymology
- Humans
- Infant
- Male
- Metabolism, Inborn Errors -- enzymology
- Mitochondria -- enzymology
- Mitochondria, Liver -- enzymology
- Mitochondria, Muscle -- enzymology
- Mitochondrial ADP, ATP Translocases -- deficiency
- NAD(P)H Dehydrogenase (Quinone)
- Oxidative Phosphorylation
- Quinone Reductases -- deficiency
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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