Spinocerebellar ataxia type 4 (Q101101)

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Spinocerebellar ataxia type 4 (SCA4) is a very rare progressive and untreatable subtype of type I autosomal dominant cerebellar ataxia (ADCA type I) characterised by ataxia with sensory neuropathy.
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ID_1686006145
    English
    Spinocerebellar ataxia type 4
    Spinocerebellar ataxia type 4 (SCA4) is a very rare progressive and untreatable subtype of type I autosomal dominant cerebellar ataxia (ADCA type I) characterised by ataxia with sensory neuropathy.

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      CID11:ID_1686006145
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      dki-india-ID_1686006145
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      Concluído
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      15 August 2026
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