Mitochondrial coupling defect in Charcot-Marie-Tooth type 2A disease. [electronic resource]
Producer: 20070626Description: 315-23 p. digitalISSN:- 0364-5134
- Adenosine Triphosphate -- metabolism
- Adult
- Apoptosis
- Cells, Cultured
- Charcot-Marie-Tooth Disease -- complications
- DNA Mutational Analysis
- Female
- Fibroblasts -- metabolism
- GTP Phosphohydrolases
- Genetic Predisposition to Disease
- Humans
- Male
- Membrane Potential, Mitochondrial -- genetics
- Membrane Proteins -- genetics
- Metabolic Networks and Pathways -- physiology
- Middle Aged
- Mitochondrial Diseases -- etiology
- Mitochondrial Proteins -- genetics
- Mutation, Missense
- Reactive Oxygen Species
- Skin -- pathology
- Statistics, Nonparametric
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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