Mutation in the Hair Cell Specific Gene POU4F3 Is a Common Cause for Autosomal Dominant Nonsyndromic Hearing Loss in Chinese Hans

Autosomal dominant nonsyndromic hearing loss (ADNSHL) is extremely heterogeneous. So far the genetic etiological contribution of the gene POU4F3 associated with ADNSHL has been rarely reported. In our previous study, a c.603_604delGG mutation in the hair cell specific gene POU4F3 has been identified...

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Detalles Bibliográficos
Autores principales: He, Longxia, Pang, Xiuhong, Chen, Penghui, Wu, Hao, Yang, Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5178374/
https://www.ncbi.nlm.nih.gov/pubmed/28053790
http://dx.doi.org/10.1155/2016/9890827

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5178374/
https://www.ncbi.nlm.nih.gov/pubmed/28053790
http://dx.doi.org/10.1155/2016/9890827

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