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...

Fuld beskrivelse

Saved in:
Bibliografiske detaljer
Main Authors: Xiang Dai, Jun Li, Xijiang Hu, Wenqian Cai
Format: Article
Sprog:engelsk
Udgivet: Wiley 2025-07-01
Serier:Molecular Genetics & Genomic Medicine
Fag:
Online adgang:https://doi.org/10.1002/mgg3.70122
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!