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Article

A POU3F4 Mutation Causes Nonsyndromic Hearing Loss in a Chinese X-linked Recessive Family.

Chinese medical journal - 5 Jan 2017

Du Wan, Han Ming-Kun, Wang Da-Yong, Han Bing, Zong Liang, Lan Lan, Yang Ju, Shen Qi, Xie Lin-Yi, Yu Lan, Guan Jing, Wang Qiu-Ju

Abstract excerpt

BACKGROUND: The molecular genetic research showed the association between X-linked hearing loss and mutations in POU3F4. This research aimed to identify a POU3F4 mutation in a nonsyndromic X-linked recessive hearing loss family. METHODS: A series of clinical evaluations including medical history, otologic examinations, family history, audiologic testing, and a high-resolution computed tomography scan were...

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Identifiers

PMID: 28051029
DOI: 10.4103/0366-6999.196565
PMCID: PMC5221118

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