CLEC4Mand STXBP5gene variations contribute to von Willebrand factor level variation in von Willebrand disease

Authors :: Sanders, Y.V.
van der Bom, J.G.
Isaacs, A.
Cnossen, M.H.
de Maat, M.P.M.
Laros-van Gorkom, B.A.P.
Fijnvandraat, K.
Meijer, K.
van Duijn, C.M.
Mauser-Bunschoten, E.P.
Eikenboom, J.
Leebeek, F.W.G.
Coppens, M.
Kors, A.
de Meris, J.
Nijziel, M.R.
Tamminga, R.Y.J.
Ypma, P.F.
Smiers, F.J.W.
Granzen, B.
Hamulyák, K.
Brons, P.
Source :: Journal of Thrombosis and Haemostasis; June 2015, Vol. 13 Issue: 6 p956-966, 11p
Publication Year :: 2015
Abstract: von Willebrand factor (VWF) levels in healthy individuals are influenced by variations in genetic loci other than the VWFgene, whose contribution to VWF levels in patients with von Willebrand disease (VWD) is largely unknown.

Full Text Access

Tools