GJB2, SLC26A4 , and mitochondrial DNA12S rRNA hot-spots in 156 subjects with non-syndromic hearing loss in Tengzhou, China.

Conclusion: In this cohort of 156 non-syndromic hearing-impaired subjects of Tengzhou area, the most common deafness-associated genesGJB2,SLC26A4andmtDNA 12S rRNAwere investigated by SNPscan efficiently.GJB2c.235delC andSLC26A4c.IVS7-2A > G were the most common mutation sites.Objectives: Until now,...

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Publicado en:	Acta Oto-Laryngologica Vol. 136; no. 8; pp. 800 - 806
Autores principales:	Ma, Yalin, Xiao, Yun, Bai, Xiaohui, Zhang, Fengguo, Zhang, Daogong, Xu, Xinmao, Xu, Lei, Wang, Haibo
Formato:	research tables/charts Journal Article
Publicado:	Taylor & Francis Ltd Aug2016
Acceso en línea:	Ver este registro en EBSCOhost