Open AccessComparison of the Mutation Spectrum of Common Deafness-Causing Genes in 509 Patients With Nonsyndromic Hearing Loss in 4 Different Areas of China by Matrix-Assisted Laser Desorption/Ionization Time-of-Flight Mass Spectrometry
Author(s) -
Yi Wang,
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WenCheng Chen,
Zhizhong Liu,
Wen Xing,
Haiyan Zhang,
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Publication year - 2021
Publication title -
pubmed central
Language(s) - English
Resource type - Journals
eISSN - 2148-3817
DOI - 10.5152/iao.2021.21086
Subject(s) - medicine , mutation , china , hearing loss , pediatrics , genetics , gene , audiology , biology , political science , law
The aim of this study is to compare the spectrum and frequency of GJB2, SLC26A4, GJB3, and MT-RNR1 mutations in 4 different areas of China.