Efficiency of microarray and SNPscan for the detection of hearing loss gene in 71 cases with nonsyndromic hearing loss

We aim to screen the mutations of 3 hearing loss (HL) genes (GJB2, SLC26A4, and 12S rRNA) in 71 cases with nonsyndromic hearing loss (NSHL) using microarray and SNPscan, and identify the roles of nonhotspot mutation of these genes in the screening of NSHL. Seventy-one cases with moderate or severe n...

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Detalles Bibliográficos
Autores principales: Han, Rui, Li, Linge, Duan, Ling, Xia, Yan, Kuyaxi, Pilidong, Zhao, Juan, Zhao, Qi, Zhang, Hua, Chen, Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2017
Materias:
6000
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5484198/
https://www.ncbi.nlm.nih.gov/pubmed/28640090
http://dx.doi.org/10.1097/MD.0000000000007149

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5484198/
https://www.ncbi.nlm.nih.gov/pubmed/28640090
http://dx.doi.org/10.1097/MD.0000000000007149

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