Identification of Novel LOXHD1 Variants in Chinese Patients with Non-Syndromic Hearing Loss

Objectives Although LOXHD1 mutations have been increasingly implicated in late-onset hereditary hearing loss, the genetic spectrum and underlying molecular mechanisms in the Chinese population remain inadequately characterized. This study aims to delineate the genetic landscape of LOXHD1 in Chinese...

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Detalhes bibliográficos

Principais autores:	Kun Zhang, Xijian Xin, Shiqi Huang, Bo Hou, Xinbo Xu, Peng Qu, Xiao Han, Hanbing Zhang
Formato:	Artigo
Idioma:	Inglês
Publicado em:	Tsinghua University Press 2026-04-01
coleção:	Journal of Otology
Assuntos:	loxhd1 variant nonsyndromic hearing loss whole-exome sequencing cochlear implants
Acesso em linha:	https://www.sciopen.com/article/10.26599/JOTO.2026.9540055
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