A novel mutation in POU3F4 in a Chinese family with X-linked non-syndromic hearing loss

OBJECTIVE: Based on the clinical manifestations of a hearing loss patient, the POU3F4 gene was tested for diagnosis of etiology. METHODS: A comprehensive physical examination was performed on the proband to exclude abnormalities of other organs, and detailed audiological testing and temporal bone CT...

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Detalles Bibliográficos
Autores principales: Huang, Bang-qing, Zeng, Jia-ling, Yuan, Yong-yi, Dai, Pu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chinese PLA General Hospital 2015
Materias:
Original article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6002573/
https://www.ncbi.nlm.nih.gov/pubmed/29937786
http://dx.doi.org/10.1016/j.joto.2015.09.004

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6002573/
https://www.ncbi.nlm.nih.gov/pubmed/29937786
http://dx.doi.org/10.1016/j.joto.2015.09.004

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