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Article

GJB2 gene mutations causing familial hereditary deafness in Turkey.

International journal of pediatric otorhinolaryngology - 1 Dec 2003

Bayazit Yildirim A, Cable Benjamin B, Cataloluk Osman, Kara Cengiz, Chamberlin Parker, Smith Richard J H, Kanlikama Muzaffer, Ozer Enver, Cakmak Ecir Ali, Mumbuc Semih, Arslan Ahmet

Abstract excerpt

Mutations in Connexin 26 (Cx26) play an important role in autosomal non-syndromic hereditary hearing loss. In this study, our objective was to find out the significance of Cx26 mutations in Turkish families who had hereditary deafness. Fourteen families who had at least two prelingually deaf chil...

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Source

Identifiers

PMID: 14643477
DOI: 10.1016/j.ijporl.2003.08.003

Genes

GJB2

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-14643477-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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