Rare Coding Variation and Risk of Intracerebral Hemorrhage

BACKGROUND AND PURPOSE: Intracerebral hemorrhage (ICH) has a substantial genetic component. We performed a preliminary search for rare coding variants associated with ICH. METHODS: 757 cases and 795 controls were genotyped using the Illumina HumanExome Beadchip (Illumina, Inc. San Diego, CA, USA). M...

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Detaylı Bibliyografya
Yayımlandı:Stroke
Asıl Yazarlar: Radmanesh, Farid, Falcone, Guido J., Anderson, Christopher D., McWilliams, David, Devan, William J., Brown, W Mark, Battey, Thomas W. K., Ayres, Alison M., Raffeld, Miriam R., Schwab, Kristin, Sun, Guangyun, Deka, Ranjan, Viswanathan, Anand, Goldstein, Joshua N., Greenberg, Steven M., Tirschwell, David L., Silliman, Scott L., Selim, Magdy, Meschia, James F., Brown, Devin L., Worrall, Bradford B., Langefeld, Carl D., Woo, Daniel, Rosand, Jonathan
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2015
Konular:
Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4519408/
https://ncbi.nlm.nih.gov/pubmed/26111891
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/STROKEAHA.115.009838
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