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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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Publicat a:Biomed Res Int
Autors principals: Hosoya, Makoto, Fujioka, Masato, Okano, Hideyuki, Ogawa, Kaoru
Format: Artigo
Idioma:Inglês
Publicat: Hindawi Publishing Corporation 2016
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Accés en línia: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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