No abstract available
MeSH terms
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Diagnosis, Differential
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Electron Transport Complex I
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Humans
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Mitochondria / enzymology
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NADH Dehydrogenase / genetics
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NADH, NADPH Oxidoreductases / genetics
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Optic Atrophy, Hereditary, Leber* / genetics
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Optic Atrophy, Hereditary, Leber* / physiopathology
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Point Mutation
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Prognosis
Substances
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NADH, NADPH Oxidoreductases
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NADH Dehydrogenase
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Electron Transport Complex I