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Article

The Prevalence of Gap Junction Protein Beta 2 (GJB2) Mutations in Non Syndromic Sensorineural Hearing Loss in Çukurova Region.

The journal of international advanced otology - 1 Aug 2015

Bozdoğan Sevcan Tuğ, Kuran Gökhan, Yüregir Özge Özalp, Aslan Hüseyin, Haytoğlu Süheyl, Ayaz Akif, Arıkan Osman Kürşat

Abstract excerpt

OBJECTIVE: To date, studies in all populations showed that mutations in the gene of Gap junction protein beta 2 (GJB2) play an important role in non-syndromic autosomal recessive congenital hearing loss. The aim of this study was to evaluate GJB2 gene of patients with hearing loss in our region using deoxyribonucleic acid (DNA) sequencing method and to demonstrate region-specific mutation and polymorphism...

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Source

Identifiers

PMID: 26381000
DOI: 10.5152/iao.2015.1212

Genes

GJB2

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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