ZNF644

Clinical relevance

Mutations in the ZNF644 gene have been found in sporadic cases of high myopia.[6]

References

  1. GRCh38: Ensembl release 89: ENSG00000122482 - Ensembl, May 2017
  2. GRCm38: Ensembl release 89: ENSMUSG00000049606 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. "Entrez Gene: zinc finger protein 644".
  6. Shi, Yi (2011). "Exome Sequencing Identifies ZNF644 Mutations in High Myopia". PLOS Genetics. 7 (6): e1002084. doi:10.1371/journal.pgen.1002084. PMC 3111487. PMID 21695231.

Further reading

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