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Article

Prevalence and range of GJB2 and SLC26A4 mutations in patients with autosomal recessive non‑syndromic hearing loss.

Molecular medicine reports - 1 Jul 2014

Jiang Hua, Chen Jia, Shan Xin-Ji, Li Ying, He Jian-Guo, Yang Bei-Bei

Abstract excerpt

The frequency and distribution of genetic mutations that cause deafness differ significantly according to ethnic group and region. Zhejiang is a province in the southeast of China, with an exceptional racial composition of the population caused by mass migration in ancient China. The purpose of the present study was to investigate the prevalence and spectrum of gap junction‑β2 (GJB2), solute carrier family 26...

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Cohort Studies
Connexin 26
Connexins
Hearing Loss, Sensorineural
Membrane Transport Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Sulfate Transporters

Tomography, X-Ray Computed

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Identifiers

PMID: 24737404
DOI: 10.3892/mmr.2014.2148

Genes

GJB2
GJB3

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

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