A Novel Nonsense Mutation of POU4F3 Gene Causes Autosomal Dominant Hearing Loss

POU4F3 gene encodes a transcription factor which plays an essential role in the maturation and maintenance of hair cells in cochlea and vestibular system. Several mutations of POU4F3 have been reported to cause autosomal dominant nonsyndromic hearing loss in recent years. In this study, we describe...

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Detalles Bibliográficos
Autores principales: Zhang, Chi, Wang, Mingming, Xiao, Yun, Zhang, Fengguo, Zhou, Yicui, Li, Jianfeng, Zheng, Qingyin, Bai, Xiaohui, Wang, Haibo
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/PMC5143711/
https://www.ncbi.nlm.nih.gov/pubmed/27999687
http://dx.doi.org/10.1155/2016/1512831

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5143711/
https://www.ncbi.nlm.nih.gov/pubmed/27999687
http://dx.doi.org/10.1155/2016/1512831

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