Spinocerebellar ataxia type 6 (Q101078): Difference between revisions

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15 August 2026
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Latest revision as of 17:52, 16 August 2026

Spinocerebellar ataxia type 6 is a common subtype of autosomal dominant cerebellar ataxia type 3, most commonly seen in Japan, Korea, the Netherlands and Germany, characterised by late-onset and slowly progressive gait ataxia, cerebellar signs and eye movement problems and caused by mutations in the CACNA1A gene.
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ID_1056119281
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    Spinocerebellar ataxia type 6
    Spinocerebellar ataxia type 6 is a common subtype of autosomal dominant cerebellar ataxia type 3, most commonly seen in Japan, Korea, the Netherlands and Germany, characterised by late-onset and slowly progressive gait ataxia, cerebellar signs and eye movement problems and caused by mutations in the CACNA1A gene.

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      CID11:ID_1056119281
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      dki-india-ID_1056119281
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      Concluído
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      15 August 2026
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