Mutation analysis of common deafness genes among 1,201 patients with non‐syndromic hearing loss in Shanxi Province

BACKGROUND: Hearing impairment is one of most frequent birth defects, which affects nearly 1 in every 1,000 live births. However, the molecular etiology of non‐syndromic deafness in China is not well studied. Here, we have investigated the presence of mutations in three genes commonly mutated in non...

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Detalles Bibliográficos
Autores principales: Zhou, Yongan, Li, Chao, Li, Min, Zhao, Zhonghua, Tian, Shuxiong, Xia, Hou, Liu, Peixian, Han, Yaxin, Ren, Ruirui, Chen, Jianping, Jia, Caihong, Guo, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6418354/
https://www.ncbi.nlm.nih.gov/pubmed/30693673
http://dx.doi.org/10.1002/mgg3.537

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6418354/
https://www.ncbi.nlm.nih.gov/pubmed/30693673
http://dx.doi.org/10.1002/mgg3.537

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