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

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

PurposeThe 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.Met...

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Bibliographic Details
Main Authors: Luhang Cai, Ya Liu, Yaping Xu, Hang Yang, Lihui Lv, Yang Li, Qiongqiong Chen, Xiaojiang Lin, Yihui Yang, Guangwei Hu, Guofeng Zheng, Jing Zhou, Qiyong Qian, Mei-ai Xu, Jin Fang, Jianjun Ding, Wei Chen, Jiong Gao
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-07-01
Series:Frontiers in Genetics
Subjects:
deafness
hearing screening
genetic screening
genetic deafness
newborn deafness
Online Access:https://www.frontiersin.org/articles/10.3389/fgene.2021.637096/full

Internet

https://www.frontiersin.org/articles/10.3389/fgene.2021.637096/full

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