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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Detalles Bibliográficos
Autores principales: Hosoya, Makoto, Fujioka, Masato, Okano, Hideyuki, Ogawa, Kaoru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4923552/
https://www.ncbi.nlm.nih.gov/pubmed/27403418
http://dx.doi.org/10.1155/2016/1781894

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4923552/
https://www.ncbi.nlm.nih.gov/pubmed/27403418
http://dx.doi.org/10.1155/2016/1781894

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