
ZNF592 Polyclonal Antibody detects endogenous levels of ZNF592 protein.
zinc finger protein 592(ZNF592) Homo sapiens 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]
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