Genetic variants at 9p21.3 are associated with risk of esophageal squamous cell carcinoma in a Chinese population

Genome‐wide association studies have linked genetic variants at 9p21.3 to the risk of multiple cancers. However, the roles of genetic variants at 9p21.3 in esophageal squamous cell carcinoma (ESCC) development are largely unknown. We evaluated the genetic variants at 9p21.3 reported in cancer genome...

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Detalles Bibliográficos
Autores principales: Lin, Xiaoming, Yan, Caiwang, Gao, Yong, Du, Jiangbo, Zhu, Xun, Yu, Fei, Huang, Tongtong, Dai, Juncheng, Ma, Hongxia, Jiang, Yue, Yin, Rong, Hu, Zhibin, Jin, Guangfu, Xu, Lin, Shen, Hongbing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5329157/
https://www.ncbi.nlm.nih.gov/pubmed/27960044
http://dx.doi.org/10.1111/cas.13130

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5329157/
https://www.ncbi.nlm.nih.gov/pubmed/27960044
http://dx.doi.org/10.1111/cas.13130

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