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

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, ot...

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Vydáno v:Chin Med J (Engl)
Hlavní autoři: 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
Médium: Artigo
Jazyk:Inglês
Vydáno: Medknow Publications & Media Pvt Ltd 2017
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Original Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5221118/
https://ncbi.nlm.nih.gov/pubmed/28051029
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0366-6999.196565
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