Biallelic Mutations in the Otogelin‐Like Gene ( OTOGL ) Associated With Congenital Non‐Syndromic Sensorineural Hearing Loss in a Chinese Family
Sign Up to like & getrecommendations! Published in 2025 at "Molecular Genetics & Genomic Medicine"
DOI: 10.1002/mgg3.70122
Abstract: 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… read more here.
Keywords: loss; non syndromic; sensorineural hearing; hearing loss ... See more keywords