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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
Barrientos, Antoni; Casademont, Jordi; Genís, David; Cardellach, Francesc; Fernández-Real, José Manuel
; et al.
Human Mutation; Hoboken Vol. 10, Iss. 3, (1997): 212.
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