Multi-Center in-Depth Screening of Neonatal Deafness Genes: Zhejiang, China

PURPOSE: The conventional genetic screening for deafness involves 9–20 variants from four genes. This study expands screening to analyze the mutation types and frequency of hereditary deafness genes in Zhejiang, China, and explore the significance of in-depth deafness genetic screening in newborns....

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Detalles Bibliográficos
Autores principales: Cai, Luhang, Liu, Ya, Xu, Yaping, Yang, Hang, Lv, Lihui, Li, Yang, Chen, Qiongqiong, Lin, Xiaojiang, Yang, Yihui, Hu, Guangwei, Zheng, Guofeng, Zhou, Jing, Qian, Qiyong, Xu, Mei-ai, Fang, Jin, Ding, Jianjun, Chen, Wei, Gao, Jiong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8282931/
https://www.ncbi.nlm.nih.gov/pubmed/34276761
http://dx.doi.org/10.3389/fgene.2021.637096

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8282931/
https://www.ncbi.nlm.nih.gov/pubmed/34276761
http://dx.doi.org/10.3389/fgene.2021.637096

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