Spinocerebellar ataxia type 35 (Q101096): Difference between revisions

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Spinocerebellar ataxia type 35 is a subtype of autosomal dominant cerebellar ataxia type 1 characterised by the adult-onset of progressive gait and limb ataxia, dysarthria, ocular dysmetria, tremor, hyperreflexia and torticollis.
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    Spinocerebellar ataxia type 35
    Spinocerebellar ataxia type 35 is a subtype of autosomal dominant cerebellar ataxia type 1 characterised by the adult-onset of progressive gait and limb ataxia, dysarthria, ocular dysmetria, tremor, hyperreflexia and torticollis.

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