No abstract available
MeSH terms
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Adult
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Ataxia / genetics
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Child
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DNA Mutational Analysis
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Disease Progression
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Energy Metabolism / genetics
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Female
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GTP Phosphohydrolases / genetics*
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Genetic Markers / genetics
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Genetic Predisposition to Disease / genetics*
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Genetic Testing
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Genotype
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Hearing Loss, Sensorineural / genetics*
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Hearing Loss, Sensorineural / pathology
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Hearing Loss, Sensorineural / physiopathology
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Humans
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Male
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Mitochondria / genetics
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Mitochondria / pathology
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Mitochondrial Diseases / genetics*
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Mitochondrial Diseases / pathology
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Mitochondrial Diseases / physiopathology
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Muscle Weakness / genetics
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Mutation / genetics*
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Optic Atrophy, Autosomal Dominant / genetics*
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Optic Atrophy, Autosomal Dominant / pathology
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Optic Atrophy, Autosomal Dominant / physiopathology
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Pedigree
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Phenotype
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Somatosensory Disorders / genetics
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Syndrome
Substances
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Genetic Markers
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GTP Phosphohydrolases
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OPA1 protein, human