Multiple sclerosis-like disorder in OPA1-related autosomal dominant optic atrophy. [electronic resource]
Producer: 20080619Description: 1152-3 p. digitalISSN:- 1526-632X
- Adult
- Brain -- metabolism
- DNA Mutational Analysis
- Diagnosis, Differential
- Energy Metabolism -- genetics
- GTP Phosphohydrolases -- genetics
- Genetic Markers -- genetics
- Genetic Predisposition to Disease -- genetics
- Genotype
- Heterozygote
- Humans
- Magnetic Resonance Imaging
- Male
- Mitochondria -- genetics
- Mitochondrial Diseases -- genetics
- Multiple Sclerosis -- genetics
- Mutation -- genetics
- Nerve Fibers, Myelinated -- metabolism
- Optic Atrophy, Autosomal Dominant -- genetics
- Optic Nerve -- metabolism
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Publication Type: Case Reports; Journal Article
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