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Article

[Prevalence of common genetic mutations and clinical characteristics analysis in patients at different ages with nonsyndromic hearing impairment].

Yi chuan = Hereditas - 1 Mar 2013

Zhang Chu-Qin, Chen Bo-Bei, Chen Ying-Ying, Liu Xue-Jun, Zheng Jing, Gao Jin-Jian, Huang Sai-Yu, Nan Ben-Yu, Zhang Yu-Yao, Yu Xiao, Guan Min-Xin

Abstract excerpt

To evaluate the correlation between genetic mutations and the age in nonsyndromic hearing impairment (NSHI) and the clinical characteristics of NSHI, 215 patients with NSHI were enrolled between April 2006 and April 2012. All patients were divided into four groups according to ages of hearing loss onset and clinic presentation (0-3, 3-6, 6-18 and 18+ years). The mutations of GJB2 and mitochondria DNA (mtDNA)...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 23575541
DOI: 10.3724/sp.j.1005.2013.00352

Genes

GJB2

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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