Biallelic Mutations in the Otogelin‐Like Gene (OTOGL) Associated With Congenital Non‐Syndromic Sensorineural Hearing Loss in a Chinese Family

ABSTRACT Background Hearing loss, characterized by significant genetic heterogeneity, is a widespread global disorder. Mutations in the OTOG and OTOGL genes have recently been implicated in non‐syndromic sensorineural hearing loss. However, the mutation spectrum of OTOGL and its functional relevance...

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Главные авторы: Xiang Dai, Jun Li, Xijiang Hu, Wenqian Cai
Формат: Статья
Язык:английский
Опубликовано: Wiley 2025-07-01
Серии:Molecular Genetics & Genomic Medicine
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Online-ссылка:https://doi.org/10.1002/mgg3.70122
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