Spinocerebellar ataxia type 4 (Q101101): Difference between revisions

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Revision as of 17:54, 16 August 2026

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
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    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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      dki-india-ID_1686006145
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