Classical mitochondrial phenotypes without mtDNA mutations: the possible role of nuclear genes. [electronic resource]
Producer: 20040924Description: 1144-7 p. digitalISSN:- 1526-632X
- Cell Nucleus -- genetics
- DNA Mutational Analysis
- DNA, Mitochondrial -- genetics
- Electron Transport Complex IV -- analysis
- Female
- Humans
- Male
- Middle Aged
- Mitochondrial Diseases -- diagnosis
- Muscle Fibers, Skeletal -- chemistry
- Mutation
- Ophthalmoplegia, Chronic Progressive External -- diagnosis
- Phenotype
- Polymerase Chain Reaction
- Polymorphism, Restriction Fragment Length
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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