Spinocerebellar ataxia type 25 (Q101077): Difference between revisions

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Revision as of 17:52, 16 August 2026

Spinocerebellar ataxia type 25 (SCA25) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterised by cerebellar ataxia and prominent sensory neuropathy.
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ID_8347192
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    Spinocerebellar ataxia type 25
    Spinocerebellar ataxia type 25 (SCA25) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterised by cerebellar ataxia and prominent sensory neuropathy.

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      CID11:ID_8347192
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