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Article

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

BioMed research international - 1 Jan 2016

Hosoya Makoto, Fujioka Masato, Okano Hideyuki, Ogawa Kaoru

Abstract excerpt

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 patterns are different between mouse and rat cochleae; the pattern in humans has not been fully investigated. We...

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Identifiers

PMID: 27403418
DOI: 10.1155/2016/1781894
PMCID: PMC4923552

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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