GJB2 Mutation Spectrum and Genotype-Phenotype Correlation in 1067 Han Chinese Subjects with Non-Syndromic Hearing Loss

GJB2 Mutation Spectrum and Genotype-Phenotype Correlation in 1067 Han Chinese Subjects with Non-Syndromic Hearing Loss

Mutations in Gap Junction Beta 2 (GJB2) have been reported to be a major cause of non-syndromic hearing loss in many populations worldwide. The spectrums and frequencies of GJB2 variants vary substantially among different ethnic groups, and the genotypes among these populations remain poorly underst...

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Bibliographic Details
Main Authors: Zheng, Jing, Ying, Zhengbiao, Cai, Zhaoyang, Sun, Dongmei, He, Zheyun, Gao, Yinglong, Zhang, Ting, Zhu, Yi, Chen, Ye, Guan, Min-Xin
Format: Online
Language:English
Published: Public Library of Science 2015
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4456361/

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https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4456361/

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