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Article

Connexin 26 gene mutations in non-syndromic hearing loss among Kuwaiti patients.

Medical principles and practice : international journal of the Kuwait University, Health Science Centre - 1 Jan 2014

Al-Sebeih Khalid, Al-Kandari Marium, Al-Awadi Sadika A, Hegazy Fatma F, Al-Khamees Ghada A, Naguib Kamal K, Al-Dabbous Reem M

Abstract excerpt

OBJECTIVE: To study connexin 26 (Cx26) gene mutations among autosomal recessive non-syndromal hearing loss in Kuwaiti patients and evaluate their effect on phenotypes. SUBJECTS AND METHODS: This cross sectional study included 100 patients aged between 6 months and 18 years, who were referred to the Sheikh Salem Al-Ali Centre for audiology and speech evaluation of autosomal recessive non-syndromic sensorineural...

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Identifiers

PMID: 24080506
DOI: 10.1159/000348304
PMCID: PMC5586821

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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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