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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Vydáno v:Biomed Res Int
Hlavní autoři: Zhang, Fengguo, Xiao, Yun, Xu, Lei, Zhang, Xue, Zhang, Guodong, Li, Jianfeng, Lv, Huaiqing, Bai, Xiaohui, Wang, Haibo
Médium: Artigo
Jazyk:Inglês
Vydáno: Hindawi Publishing Corporation 2016
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Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4876198/
https://ncbi.nlm.nih.gov/pubmed/27247933
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2016/1302914
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