Molecular epidemiology of Chinese Han deaf patients with bi-allelic and mono-allelic GJB2 mutations | Orphanet Journal of Rare Diseases | Full Text

Molecular epidemiology of Chinese Han deaf patients with bi-allelic and mono-allelic GJB2 mutations | Orphanet Journal of Rare Diseases | Full Text

Molecular epidemiology of Chinese Han deaf patients with bi-allelic and mono-allelic GJB2 mutations

Recessive mutations in GJB2 is the most common cause of genetic hearing loss worldwide. The aim of this study is to determine the spectrum and frequency of GJB2 variants in Chinese Han deaf patients and to invest...

Authors:Xiaoyu Yu, Yun Lin, Jun Xu, Tuanjie Che, Lin Li, Tao Yang and Hao Wu

Citation:Orphanet Journal of Rare Diseases 2020 15:29

Content type:Research

Published on: 28 January 2020

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