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Distinct Expression Pattern of a Deafness Gene, KIAA1199, in a Primate Cochlea

Deafness is one of the most common types of congenital impairments, and at least half of the cases are caused by hereditary mutations. Mutations of the gene KIAA1199 are associated with progressive hearing loss. Its expression is abundant in human cochlea, but interestingly the spatial expression pa...

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Detalhes bibliográficos
Publicado no:Biomed Res Int
Main Authors: Hosoya, Makoto, Fujioka, Masato, Okano, Hideyuki, Ogawa, Kaoru
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi Publishing Corporation 2016
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4923552/
https://ncbi.nlm.nih.gov/pubmed/27403418
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2016/1781894
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