Identification of TMPRSS3 as a Significant Contributor to Autosomal Recessive Hearing Loss in the Chinese Population

Hereditary hearing loss is characterized by a high degree of genetic heterogeneity. Mutations in the TMPRSS3 (transmembrane protease, serine 3) gene cause prelingual (DFNB10) or postlingual (DFNB8) deafness. In our previous study, three pathogenic mutations in TMPRSS3 were identified in one Chinese...

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Detalles Bibliográficos
Autores principales: Gao, Xue, Huang, Sha-Sha, Yuan, Yong-Yi, Xu, Jin-Cao, Gu, Ping, Bai, Dan, Kang, Dong-Yang, Han, Ming-Yu, Wang, Guo-Jian, Zhang, Mei-Guang, Li, Jia, Dai, Pu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5485344/
https://www.ncbi.nlm.nih.gov/pubmed/28695016
http://dx.doi.org/10.1155/2017/3192090

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5485344/
https://www.ncbi.nlm.nih.gov/pubmed/28695016
http://dx.doi.org/10.1155/2017/3192090

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