Screening of deafness-causing DNA variants that are common in patients of European ancestry using a microarray-based approach

The unparalleled heterogeneity in genetic causes of hearing loss along with remarkable differences in prevalence of causative variants among ethnic groups makes single gene tests technically inefficient. Although hundreds of genes have been reported to be associated with nonsyndromic hearing loss (N...

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Detalles Bibliográficos
Autores principales: Yan, Denise, Xiang, Guangxin, Chai, Xingping, Qing, Jie, Shang, Haiqiong, Zou, Bing, Mittal, Rahul, Shen, Jun, Smith, Richard J. H., Fan, Yao-Shan, Blanton, Susan H., Tekin, Mustafa, Morton, Cynthia, Xing, Wanli, Cheng, Jing, Liu, Xue Zhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5342170/
https://www.ncbi.nlm.nih.gov/pubmed/28273078
http://dx.doi.org/10.1371/journal.pone.0169219

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5342170/
https://www.ncbi.nlm.nih.gov/pubmed/28273078
http://dx.doi.org/10.1371/journal.pone.0169219

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