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Article

The Analysis of GJB2, GJB3, and GJB6 Gene Mutations in Patients with Hereditary Non-Syndromic Hearing Loss Living in Sivas.

The journal of international advanced otology - 1 Dec 2019

Küçük Kurtulgan Hande, Altuntaş Emine Elif, Yıldırım Malik Ejder, Özdemir Öztürk, Bağcı Binnur, Sezgin İlhan

Abstract excerpt

OBJECTIVES: The aim of the present study was to investigate the presence of GJB2, GJB3, and GJB6 gene mutations in non-syndromic sensorineural hearing loss (NSHL) cases living in Sivas region, to provide appropriate genetic counseling for cases who were found to have mutation, and to contribute to decrease the frequency of mutant allele in the next generation and plan treatment and rehabilitation with early...

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Identifiers

PMID: 31846914
DOI: 10.5152/iao.2019.5401
PMCID: PMC6937194

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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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