MNX1

Clinical significance

Mutations in the MNX1 gene are associated with Currarino syndrome.[5]

References

  1. GRCh38: Ensembl release 89: ENSG00000130675 - Ensembl, May 2017
  2. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Entrez Gene: HLXB9 homeobox HB9".
  5. Merello E, De Marco P, Ravegnani M, Riccipetitoni G, Cama A, Capra V (2013). "Novel MNX1 mutations and clinical analysis of familial and sporadic Currarino cases". Eur J Med Genet. 56 (12): 648–54. doi:10.1016/j.ejmg.2013.09.011. PMID 24095820.

Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.


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