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

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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Bibliographic Details
Main Authors: Wan Du, Ming-Kun Han, Da-Yong Wang, Bing Han, Liang Zong, Lan Lan, Ju Yang, Qi Shen, Lin-Yi Xie, Lan Yu, Jing Guan, Qiu-Ju Wang
Format: Article
Language:English
Published: Wolters Kluwer 2017-01-01
Series:Chinese Medical Journal
Subjects:
c.499C>T; Nonsyndromic Hearing Loss; POU3F4; X-linked
Online Access:http://www.cmj.org/article.asp?issn=0366-6999;year=2017;volume=130;issue=1;spage=88;epage=92;aulast=Du

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http://www.cmj.org/article.asp?issn=0366-6999;year=2017;volume=130;issue=1;spage=88;epage=92;aulast=Du

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