Whole exome-wide association study identifies a missense variant in SLC2A4RG associated with glioblastoma risk

In this study, we conducted a genome-wide scan of single nucleotide polymorphisms (SNPs) to identify coding variants that is associated with the risk of glioblastoma (GBM), the most common and most malignant subtype of glioma. We genotyped 1038 GBM cases and 1008 controls in a Chinese Han population...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Am J Cancer Res
Prif Awduron: Zhao, Yingjie, Yun, Dapeng, Zou, Xiang, Jiang, Tao, Li, Gang, Hu, Lingna, Chen, Juxiang, Xu, Jianfeng, Mao, Ying, Chen, Hongyan, Lu, Daru
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: e-Century Publishing Corporation 2017
Pynciau:
Original Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC5622227/
https://ncbi.nlm.nih.gov/pubmed/28979815
Tagiau: Ychwanegu Tag
Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!

Eitemau Tebyg