Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China

ObjectiveThis study aimed to delineate the prevalence and mutation spectrum of deafness-associated genes among newborns in a resource-limited region of China, and to assess the diagnostic yield of combined hearing and genetic screening.MethodsFrom May 2017 to May 2023, 22,819 newborns underwent conc...

وصف كامل

التفاصيل البيبلوغرافية

المؤلفون الرئيسيون:	Qin She, Hui-Lin Ou, Er-Fang Tang, Wei Huang, Wei-He Tan, Mu-Lan Zeng, Xiu-Feng Pan, Chen-Bing Liu
التنسيق:	Artigo
اللغة:	Inglês
منشور في:	Frontiers Media S.A. 2026-06-01
سلاسل:	Frontiers in Genetics
الموضوعات:	genetic screening for deafness GJB2 gene mutations neonatal hearing screening resource-limited regions whole exome sequencing (WES)
الوصول للمادة أونلاين:	https://www.frontiersin.org/articles/10.3389/fgene.2026.1873535/full
الوسوم:	إضافة وسم لا توجد وسوم, كن أول من يضع وسما على هذه التسجيلة!