A POU3F4 Mutation Causes Nonsyndromic Hearing Loss in a Chinese X-linked Recessive Family

BACKGROUND: The molecular genetic research showed the association between X-linked hearing loss and mutations in POU3F4. This research aimed to identify a POU3F4 mutation in a nonsyndromic X-linked recessive hearing loss family. METHODS: A series of clinical evaluations including medical history, ot...

Descripción completa

Detalles Bibliográficos
Autores principales: Du, Wan, Han, Ming-Kun, Wang, Da-Yong, Han, Bing, Zong, Liang, Lan, Lan, Yang, Ju, Shen, Qi, Xie, Lin-Yi, Yu, Lan, Guan, Jing, Wang, Qiu-Ju
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5221118/
https://www.ncbi.nlm.nih.gov/pubmed/28051029
http://dx.doi.org/10.4103/0366-6999.196565

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5221118/
https://www.ncbi.nlm.nih.gov/pubmed/28051029
http://dx.doi.org/10.4103/0366-6999.196565

Ejemplares similares