Targeted Next-Generation Sequencing in Uyghur Families with Non-Syndromic Sensorineural Hearing Loss

The mutation spectrum of deafness genes may vary in different ethnical groups. In this study, we investigated the genetic etiology of nonsyndromic deafness in four consanguineous and two multiplex Uyghur families in which mutations in common deafness genes GJB2, SLC26A4 and MT-RNR1 were excluded. Ta...

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Detalles Bibliográficos
Autores principales: Chen, Ying, Wang, Zhentao, Wang, Zhaoyan, Chen, Dongye, Chai, Yongchuan, Pang, Xiuhong, Sun, Lianhua, Wang, Xiaowen, Yang, Tao, Wu, Hao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4444116/
https://www.ncbi.nlm.nih.gov/pubmed/26011067
http://dx.doi.org/10.1371/journal.pone.0127879

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4444116/
https://www.ncbi.nlm.nih.gov/pubmed/26011067
http://dx.doi.org/10.1371/journal.pone.0127879

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