Identification of Pathogenic Genes of Nonsyndromic Hearing Loss in Uyghur Families Using Massively Parallel DNA Sequencing Technique

We aim to identify the mutations of deafness genes using massively parallel DNA sequencing in the 12 Uyghur families. SNPscan method was used to screen against the 124 sites in the common deafness genes in probands. Subjects with SNPscan negativity were subject to massively parallel DNA sequencing f...

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Detalles Bibliográficos
Autores principales: Chen, Yu, Lu, Yu, Kuyaxi, Pilidong, Cheng, Jing, Zhao, Juan, Zhao, Qi, Musha, Patiguli, Zhang, Hua, Yuan, Huijun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5859828/
https://www.ncbi.nlm.nih.gov/pubmed/29692870
http://dx.doi.org/10.1155/2018/5298057

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5859828/
https://www.ncbi.nlm.nih.gov/pubmed/29692870
http://dx.doi.org/10.1155/2018/5298057

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