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Popular science summary: Recessive mutations in STUB1 cause cerebellar ataxia Autosomal recessive cerebellar ataxias (ARCA) constitute a group of rare disorders characterized by ataxia due to cerebellum neurodegeneration. Here we characterize three novel mutations in the STUB1 (STIP1 homology and U-box containing protein) gene as the cause of ARCA in two families. STUB1 encodes CHIP (C-terminus
