CLEC4M and STXBP5 gene variations contribute to vonWillebrand factor level variation in von Willebrand disease

Sanders, Y.V.; Bom, J.G. van der; Isaacs, A.; Cnossen, M.H.; Maat, M.P.M. de; Laros-van Gorkom, B.A.P.; ... ; Win Study Grp (2015)

Article / Letter to editor

• CLEC4M protein
• human
• polymorphism
• single nucleotide
• STXBP5 protein
• von Willebrand disease
• von Willebrand factor

• All authors: Sanders, Y.V.; Bom, J.G. van der; Isaacs, A.; Cnossen, M.H.; Maat, M.P.M. de; Laros-van Gorkom, B.A.P.; Fijnvandraat, K.; Meijer, K.; Duijn, C.M. van; Mauser-Bunschoten, E.P.; Eikenboom, J.; Leebeek, F.W.G.; Win Study Grp
• Date: 2015-06-30
• Journal: Journal of Thrombosis and Haemostasis
• Volume: 13
• Issue: 6
• Pages: 956 - 966
• DOI: doi:10.1111/jth.12927