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Article

GJB2 mutations are rare in probands with hearing loss in Chinese assortative mating families.

International journal of pediatric otorhinolaryngology - 1 Feb 2014

Chen Guanming, Liu Jing, Dong Jiashu, Li Jiaxin, Fu Siqing

Abstract excerpt

OBJECTIVE: GJB2 mutation is recognized as the prevalent causes of non-syndromic hearing loss (NSHL) worldwide. However, the mutation profiles of GJB2 are rarely reported in deafness probands of the assortative mating family. Therefore, this study aimed to characterize the frequencies of GJB2 mutations in probands with hearing loss in the assortative mating family in Hubei province, Central China. METHODS: Genomic...

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Source

Identifiers

PMID: 24359977
DOI: 10.1016/j.ijporl.2013.11.013

Genes

GJB2

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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