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Article

Unraveling the Diversity of GJB2 Mutations in Nonsyndromic Hearing Loss: A Comprehensive Study in the Moroccan Population.

Audiology & neuro-otology - 1 Jan 2024

El Fizazi Khawla, Abbassi Meriame, Nmer Samira, Laamarti Hajar, ElAlami Mohamed Noureddine, Ouldim Karim, Bouguenouch Laila, Ridal Mohammed

Abstract excerpt

INTRODUCTION: Despite the high genetic heterogeneity of hearing loss, mutations in the GJB2 gene are a major cause of autosomal recessive nonsyndromic hearing loss (NSHL) worldwide. However, the mutation profile of GJB2 in NSHL is under-investigated in Morocco, especially among simplex cases. This study aimed to identify the spectrum and frequency of GJB2 mutations in the Moroccan population among simplex and...

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PMID: 38253033
DOI: 10.1159/000535346

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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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