No abstract available
MeSH terms
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Adolescent
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Electromyography
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Female
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GTP Phosphohydrolases / genetics*
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Humans
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Incidental Findings*
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Male
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Mutation*
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Ophthalmology
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Optic Atrophy, Autosomal Dominant / diagnosis*
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Optic Atrophy, Autosomal Dominant / genetics*
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Rhabdomyolysis / diagnosis
Substances
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GTP Phosphohydrolases
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OPA1 protein, human