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Article

Connexin 26 (GJB2) gene mutations linked with autosomal recessive non-syndromic sensor neural hearing loss in the Iraqi population.

Journal of medicine and life - 1 Jan 2000

Al-Janabi Anwar Madlool, Ahmmed Habeeb Shuhaib, Al-Khafaji Salih Mahdi

Abstract excerpt

Deafness is a total or partial hearing loss that may appear at any age and with different degrees of severity. Approximately 50% of hearing loss have a genetic origin, and among them, non-syndromic sensorineural deafness represents about 70% of the cases. From them, 80% correspond to autosomal recessive inheritance deafness. Autosomal recessive deafness was not studied enough at the molecular level in Iraq. This...

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Identifiers

PMID: 35126756
DOI: 10.25122/jml-2021-0152
PMCID: PMC8811675

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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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