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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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Detalhes bibliográficos
Publicado no:Neural Plast
Main Authors: He, Longxia, Pang, Xiuhong, Chen, Penghui, Wu, Hao, Yang, Tao
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi Publishing Corporation 2016
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5178374/
https://ncbi.nlm.nih.gov/pubmed/28053790
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2016/9890827
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