Exome Array Analysis of 9721 Ischemic Stroke Cases from the SiGN Consortium

Recent genome wide association studies have identified 89 common genetic variants robustly associated with ischemic stroke and primarily located in non-coding regions. To evaluate the contribution of coding variants, which are mostly rare, we performed an exome array analysis on 106,101 SNPs for 972...

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Detalles Bibliográficos
Autores principales: Xu, Huichun, Nguyen, Kevin, Gaynor, Brady J., Ling, Hua, Zhao, Wei, McArdle, Patrick F., O’Connor, Timothy D., Stine, O. Colin, Ryan, Kathleen A., Lynch, Megan, Smith, Jennifer A., Faul, Jessica D., Hu, Yao, Haessler, Jeffrey W., Fornage, Myriam, Kooperberg, Charles, Perry, James A., Hong, Charles C., Cole, John W., Pugh, Elizabeth, Doheny, Kimberly, Kardia, Sharon L. R., Weir, David R., Kittner, Steven J., Mitchell, Braxton D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9858999/
https://www.ncbi.nlm.nih.gov/pubmed/36672803
http://dx.doi.org/10.3390/genes14010061

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9858999/
https://www.ncbi.nlm.nih.gov/pubmed/36672803
http://dx.doi.org/10.3390/genes14010061

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