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Article Dans Une Revue Molecular Biology Reports Année : 2023

Novel pathogenic WHRN variant causing hearing loss in a moroccan family

Résumé

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.
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Dates et versions

hal-04281535 , version 1 (13-11-2023)

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Citer

Imane Aitraise, Ghita Amalou, Salaheddine Redouane, Hicham Charoute, Khalid Snoussi, et al.. Novel pathogenic WHRN variant causing hearing loss in a moroccan family. Molecular Biology Reports, 2023, ⟨10.1007/s11033-023-08901-8⟩. ⟨hal-04281535⟩
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