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,...
| Publicado en: | Acta Oto-Laryngologica Vol. 136; no. 8; pp. 800 - 806 |
|---|---|
| Autores principales: | , , , , , , , |
| Formato: | research tables/charts Journal Article |
| Publicado: |
Taylor & Francis Ltd
Aug2016
|
| Acceso en línea: | Ver este registro en EBSCOhost |