Genetic screening for hearing loss of 38,589 neonates with follow-up in South China

Abstract Background Hearing loss (HL) is a prevalent disease in children, and conventional neonatal hearing screening has a limited effect. The objective of this study was to analyze the frequency of frequent deafness-associated variants [GJB2, GJB3, SLC26A4, and MTRNR1 (12 S rRNA)] in neonates from...

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Główni autorzy:	Xia Gu, Runzhong Huang, Jie Xie, Congcong Shi, Yinchun Zhang, Zao Liang, Lu Wang, Dongfan Xiao, Guilong Yuan, Chuanfeng Li, Jinjin Chen, Hu Hao
Format:	Artigo
Język:	Inglês
Wydane:	BMC 2025-12-01
Seria:	Human Genomics
Hasła przedmiotowe:	Hearing loss Neonates’ hearing screening Next-generation sequencing Combined screening Follow-up research
Dostęp online:	https://doi.org/10.1186/s40246-025-00874-y
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