Sporadic cerebellar ataxia associated with hypogonadotropic hypogonadism and PNPLA6 gene mutation. Case report in a Brazilian patient

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Teive, H. A. G.
Boguszewski, C. L.
Raskin, S.
Buck, C.
Seminara, S. B.
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R74 [神经病学与精神病学];
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页码:S337 / S337
页数:1
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