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ZNF592

Official Full Name
zinc finger protein 592
Organism
Homo sapiens
GeneID
9640
Background
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]
Synonyms
CAMOS; SCAR5;

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