Whole-exome sequencing identifies rare variants in STAB2 associated with venous thromboembolic disease

Deep vein thrombosis and pulmonary embolism, collectively defined as venous thromboembolism (VTE), are the third leading cause of cardiovascular death in the United States. Common genetic variants conferring increased varying degrees of VTE risk have been identified by genome-wide association studie...

Ausführliche Beschreibung

Bibliographische Detailangaben

Veröffentlicht in:	BLOOD 2020-07, Vol.136 (5), p.533-541
Hauptverfasser:	Desch, Karl C., Ozel, Ayse B., Halvorsen, Matt, Jacobi, Paula M., Golden, Krista, Underwood, Mary, Germain, Marine, Tregouet, David-Alexandre, Reitsma, Pieter H., Kearon, Clive, Mokry, Lauren, Richards, J. Brent, Williams, Frances, Li, Jun Z., Goldstein, David, Ginsburg, David
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Cell Adhesion Molecules, Neuronal - genetics Exome Sequencing - methods Female Genetic Predisposition to Disease - genetics Genotype Humans Male Mutation Plenary Paper Venous Thromboembolism - blood Venous Thromboembolism - genetics von Willebrand Factor - metabolism
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!