Children with GJB2 gene mutations have various audiological phenotypes

The current study retrospectively investigated variations in audiological phenotypes in children with GJB2 gene mutations. Subjects were 128 infants and young children who were seen as outpatients by Otology at Beijing Tongren Hospital from 2012 to 2018. Of the 128 subjects, 99 had biallelic truncat...

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Veröffentlicht in:	BioScience Trends 2018/08/31, Vol.12(4), pp.419-425
Hauptverfasser:	Wang, Xianlei, Huang, Lihui, Zhao, Xuelei, Wang, Xueyao, Cheng, Xiaohua, Du, Yating, Liu, Dongxin
Format:	Artikel
Sprache:	eng
Schlagworte:	Child Child, Preschool Connexins - genetics Female Genotype GJB2 gene Hearing Loss, Sensorineural - genetics Humans Infant Male Mutation - genetics Phenotype screening
Online-Zugang:	Volltext
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