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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Detalhes bibliográficos

Principais autores:	Xiang Dai, Jun Li, Xijiang Hu, Wenqian Cai
Formato:	Artigo
Idioma:	Inglês
Publicado em:	Wiley 2025-07-01
coleção:	Molecular Genetics & Genomic Medicine
Assuntos:	mutations nonsyndromic hearing loss OTOGL single‐cell RNA sequencing whole exome sequencing
Acesso em linha:	https://doi.org/10.1002/mgg3.70122
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