Rare Missense Functional Variants at COL4A1 and COL4A2 in Sporadic Intracerebral Hemorrhage

OBJECTIVE: To test the genetic contribution of rare missense variants in COL4A1 and COL4A2 in which common variants are genetically associated with sporadic intracerebral hemorrhage (ICH), we performed rare variant analysis in multiple sequencing data for the risk for sporadic ICH. METHODS: We perfo...

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Publicado en:Neurology
Main Authors: Chung, Jaeyoon, Hamilton, Graham, Kim, Minsup, Marini, Sandro, Montgomery, Bailey, Henry, Jonathan, Cho, Art E., Brown, Devin L., Worrall, Bradford B., Meschia, James F., Silliman, Scott L., Selim, Magdy, Tirschwell, David L., Kidwell, Chelsea S., Kissela, Brett, Greenberg, Steven M., Viswanathan, Anand, Goldstein, Joshua N., Langefeld, Carl D., Rannikmae, Kristiina, Sudlow, Catherine L.M., Samarasekera, Neshika, Rodrigues, Mark, Al-Shahi Salman, Rustam, Prendergast, James G.D., Harris, Sarah E., Deary, Ian, Woo, Daniel, Rosand, Jonathan, Van Agtmael, Tom, Anderson, Christopher D.
Formato: Artigo
Idioma:Inglês
Publicado: Lippincott Williams & Wilkins 2021
Assuntos:
Research Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC8302151/
https://ncbi.nlm.nih.gov/pubmed/34031201
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0000000000012227
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