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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...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Hindawi Publishing Corporation
2016
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| Materias: | |
| 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 |