DFNY1
Y-vezana gluhoća vezana je za protein koji je kod ljudi kodiran genom DFNY1 Y-povezano oštećenje sluha (DFNY1, MIM 400043) jedno je od rijetkih mendelovskih bolesti koje su Y-vezane kod ljudi.[2]
DFNY1 | |||||||
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Identifikatori | |||||||
Aliasi | DFNY1 | ||||||
Vanjski ID-jevi | GeneCards: DFNY1 | ||||||
Ortolozi | |||||||
Vrste | Čovjek | Miš | |||||
Entrez |
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Ensembl |
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UniProt |
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RefSeq (mRNK) |
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RefSeq (bjelančevina) |
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Lokacija (UCSC) | n/a | n/a | |||||
PubMed pretraga | [1] | n/a | |||||
Wikipodaci | |||||||
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Reference uredi
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Entrez Gene: Deafness, Y-linked 1".
Dopunska literatura uredi
- Wang QJ, Rao SQ, Zhao YL, Liu QJ, Zong L, Han MK, Han DY, Yang WY (juni 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.
- 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 (juni 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.