Cargando…
Mutation Spectrum of Common Deafness-Causing Genes in Patients with Non-Syndromic Deafness in the Xiamen Area, China
In China, approximately 30,000 babies are born with hearing impairment each year. However, the molecular factors causing congenital hearing impairment in the Xiamen area of Fujian province have not been evaluated. To provide accurate genetic testing and counseling in the Xiamen area, we investigated...
Autores principales: | Jiang, Yi, Huang, Shasha, Deng, Tao, Wu, Lihua, Chen, Juan, Kang, Dongyang, Xu, Xiufeng, Li, Ruiyu, Han, Dongyi, Dai, Pu |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4529078/ https://www.ncbi.nlm.nih.gov/pubmed/26252218 http://dx.doi.org/10.1371/journal.pone.0135088 |
Ejemplares similares
-
Mutation spectra and founder effect of TMC1 in patients with non‐syndromic deafness in Xiamen area, China
por: Jiang, Yi, et al.
Publicado: (2017) -
Genetic mutations in nonsyndromic deafness patients of Chinese minority and han ethnicities in Yunnan, China
por: Xin, Feng, et al.
Publicado: (2013) -
Analysis of mutation spectrum of common deafness-causing genes in Hakka newborns in southern China by semiconductor sequencing
por: Zhao, Pingsen, et al.
Publicado: (2018) -
Application of a New Genetic Deafness Microarray for Detecting Mutations in the Deaf in China
por: Wu, Hong, et al.
Publicado: (2016) -
Cellular and Deafness Mechanisms Underlying Connexin Mutation-Induced Hearing Loss – A Common Hereditary Deafness
por: Wingard, Jeffrey C., et al.
Publicado: (2015)