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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Dis Markers
Prif Awduron: Chen, Yu, Lu, Yu, Kuyaxi, Pilidong, Cheng, Jing, Zhao, Juan, Zhao, Qi, Musha, Patiguli, Zhang, Hua, Yuan, Huijun
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Hindawi 2018
Pynciau:
Research Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC5859828/
https://ncbi.nlm.nih.gov/pubmed/29692870
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2018/5298057
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