Mutation Analysis of the Common Deafness Genes in Patients with Nonsyndromic Hearing Loss in Linyi by SNPscan Assay

Hearing loss is a common sensory disorder, and at least 50% of cases are due to a genetic etiology. Although hundreds of genes have been reported to be associated with nonsyndromic hearing loss, GJB2, SLC26A4, and mtDNA12SrRNA are the major contributors. However, the mutation spectrum of these commo...

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Detalles Bibliográficos
Autores principales: Zhang, Fengguo, Xiao, Yun, Xu, Lei, Zhang, Xue, Zhang, Guodong, Li, Jianfeng, Lv, Huaiqing, Bai, Xiaohui, Wang, Haibo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4876198/
https://www.ncbi.nlm.nih.gov/pubmed/27247933
http://dx.doi.org/10.1155/2016/1302914

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4876198/
https://www.ncbi.nlm.nih.gov/pubmed/27247933
http://dx.doi.org/10.1155/2016/1302914

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