Functional rare variant in a C/EBP beta binding site in NINJ2 gene increases the risk of coronary artery disease

Objective: NINJ2 regulates activation of vascular endothelial cells, and genome-wide association studies showed that variants in NINJ2 confer risk to stroke. However, whether variants in NINJ2 are associated with coronary artery disease (CAD) is unknown. Methods: We genotyped rs34166160 in NINJ2 in...

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Detalles Bibliográficos
Autores principales: Wang, Pengyun, Wang, Yifan, Peng, Huixin, Wang, Jingjing, Zheng, Qian, Wang, Pengxia, Wang, Jing, Zhang, Hongfu, Huang, Yufeng, Xiong, Liang, Zhang, Rongfeng, Xia, Yunlong, Wang, Qing K., Xu, Chengqi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2021
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8714150/
https://www.ncbi.nlm.nih.gov/pubmed/34897030
http://dx.doi.org/10.18632/aging.203755

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