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This gene is thought to play a role in a complex developmental pathway and the regulation of genes involved in cerebellar development. Mutations in this gene have been associated with autosomal recessive spinocerebellar ataxia. [provided by RefSeq, Jan 2011].
8430405N24; A730014M16Rik; CAMOS; KIAA0211; mKIAA0211; SCAR5; Zfp592; Zfp-592; Zinc finger protein 592; ZNF592
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