Deafness, Y-linked 1 (DFNY1) is a protein that in humans is encoded by the DFNY1 gene. Y-linked hearing impairment (DFNY1, MIM 400043) is one of the few Mendelian disorders showing Y-linkage in humans.[2]
| DFNY1 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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| Aliases | DFNY1, deafness, Y-linked 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||
| External IDs | GeneCards: DFNY1; OMA:DFNY1 - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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References
edit- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Entrez Gene: Deafness, Y-linked 1".
Further reading
edit- Wang QJ, Rao SQ, Zhao YL, Liu QJ, Zong L, Han MK, Han DY, Yang WY (June 2009). "The large Chinese family with Y-linked hearing loss revisited: clinical investigation". Acta Oto-Laryngologica. 129 (6): 638–43. doi:10.1080/00016480802216347. PMID 18720061. S2CID 12827389.
- Wang QJ, Lu CY, Li N, Rao SQ, Shi YB, Han DY, Li X, Cao JY, Yu LM, Li QZ, Guan MX, Yang WY, Shen Y (June 2004). "Y-linked inheritance of non-syndromic hearing impairment in a large Chinese family". Journal of Medical Genetics. 41 (6): e80. doi:10.1136/jmg.2003.012799. PMC 1735813. PMID 15173246.
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