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Article

Novel pathogenic WHRN variant causing hearing loss in a moroccan family.

Molecular biology reports - 1 Dec 2023

AitRaise Imane, Amalou Ghita, Redouane Salaheddine, Charoute Hicham, Snoussi Khalid, Abdelghaffar Houria, Bonnet Crystel, Petit Christine, Barakat Abdelhamid

Abstract excerpt

OBJECTIVES: The most prevalent sensory disease in humans is deafness. A variety of genes have been linked to hearing loss, which can either be isolated (non-syndromic) or associated with lesions in other organs (syndromic). It has been discovered that WHRN variants are responsible for non-syndromic hearing loss and Usher syndrome type II. METHODS AND RESULTS: Exome sequencing in a consanguineous Moroccan patient...

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Identifiers

PMID: 37924449
DOI: 10.1007/s11033-023-08901-8

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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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