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Article

The landscape of gene mutations in a cohort of 3353 Han Chinese children with nonsyndromic hearing loss.

EBioMedicine - 1 Apr 2026

Xiao Yun, Chen Lei, Han Yuechen, Luo Jianfen, Wang Mingming, Ai Yu, Liu Wenwen, Xiong Wenping, Jin Yu, Kong Shuhui, Xu Kaifan, Fan Zhaomin, Xu Lei, Wang Haibo

Abstract excerpt

BACKGROUND: Genetic diagnosis plays a critical role in enhancing the identification and clinical management of pediatric hearing loss, ultimately improving both physiological outcomes and social-emotional development. As one of the most prevalent sensory disorders characterized by substantial genetic heterogeneity, hearing loss requires the implementation of efficient diagnostic approaches to inform targeted...

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Identifiers

PMID: 41833579
DOI: 10.1016/j.ebiom.2026.106211
PMCID: PMC12999288

Genes

FOXI1
NEU4

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

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