
pmid: 2544896
handle: 11577/3279894
Male, Cytochrome-c Oxidase Deficiency, Neuromuscular Diseases, Syndrome, Central Nervous System Diseases; Chromosome Deletion; Cytochrome-c Oxidase Deficiency; Electron Transport Complex IV; Female; Humans; Leigh Disease; Male; Mitochondria, Muscle; Neuromuscular Diseases; Optic Atrophies, Hereditary; Syndrome, Mitochondria, Muscle, Electron Transport Complex IV, Optic Atrophies, Hereditary, Central Nervous System Diseases, Humans, Female, Chromosome Deletion, Leigh Disease
Male, Cytochrome-c Oxidase Deficiency, Neuromuscular Diseases, Syndrome, Central Nervous System Diseases; Chromosome Deletion; Cytochrome-c Oxidase Deficiency; Electron Transport Complex IV; Female; Humans; Leigh Disease; Male; Mitochondria, Muscle; Neuromuscular Diseases; Optic Atrophies, Hereditary; Syndrome, Mitochondria, Muscle, Electron Transport Complex IV, Optic Atrophies, Hereditary, Central Nervous System Diseases, Humans, Female, Chromosome Deletion, Leigh Disease
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