Zinc finger protein 592 explained

Zinc finger protein 592 is a protein that in humans is encoded by the ZNF592 gene.[1]

Function

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.

Further reading

Notes and References

  1. Web site: Entrez Gene: Zinc finger protein 592. 2016-03-07.