Autosomal recessive spinocerebellar ataxia type 12

An autosomal dominant sub-type of spinocerebellar ataxia caused by mutation(s) in the PPP2R2B gene, encoding serine/threonine-protein phosphatase 2A 55 kDa regulatory subunit B beta isoform. It presents with characteristic action tremors in the upper limbs, followed by other movement abnormalities.

Disease Alternative Name

spinocerebellar ataxia type 12

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