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Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy
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2000
Year
Neurodegenerative DiseasesMitochondrial FunctionOphthalmologyGenetic DisorderGeneticsDominant Optic AtrophyLeber Hereditary Optic NeuropathyNuclear Gene Opa1Mitochondrial Dynamin-related ProteinMolecular GeneticsDegenerative DiseaseMedicine
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