Genome-wide association study identifies locus at chromosome 2q32.1 associated with syncope and collapse

AIMS: Syncope is a common condition associated with frequent hospitalization or visits to the emergency department. Family aggregation and twin studies have shown that syncope has a heritable component. We investigated whether common genetic variants predispose to syncope and collapse. METHODS AND R...

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Detalles Bibliográficos
Autores principales: Hadji-Turdeghal, Katra, Andreasen, Laura, Hagen, Christian M, Ahlberg, Gustav, Ghouse, Jonas, Bækvad-Hansen, Marie, Bybjerg-Grauholm, Jonas, Hougaard, David M, Hedley, Paula, Haunsø, Stig, Svendsen, Jesper H, Kanters, Jørgen K, Jepps, Thomas A, Skov, Morten W, Christiansen, Michael, Olesen, Morten S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6918066/
https://www.ncbi.nlm.nih.gov/pubmed/31049583
http://dx.doi.org/10.1093/cvr/cvz106

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