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Sporadic heteroplasmic single 5.5 Kb mitochondrial DNA deletion associated with cerebellar ataxia, hypogonadotropic hypogonadism, choroidal dystrophy, and mitochondrial respiratory chain complex I deficiency

June 2, 2017 | Autor: Virginia Nunes | Categoría: Genetics, Skeletal muscle biology, Human, Mitochondrial DNA, Humans, Female, Cerebellar ataxia, Mitochondrial Respiratory Chain, Electron Transport, Pedigree, Clinical Sciences, Late onset hypogonadism, Adult, Female, Cerebellar ataxia, Mitochondrial Respiratory Chain, Electron Transport, Pedigree, Clinical Sciences, Late onset hypogonadism, Adult
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