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NCBI Description of ZNF592 |
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. |
Community Annotation of ZNF592 Add / Edit ZNF592: Annotations
No community annotations yet for ZNF592.
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Figure notes
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Data details