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

Author(s):
Sanders, Y.V.; Bom, J.G. van der (0000-0001-5251-0342); 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
Published
2015
Publication type
Article / Letter to editor
CLEC4M proteinhumanpolymorphismsingle nucleotideSTXBP5 proteinvon Willebrand diseasevon Willebrand factor
Date issued
2015-06-30
Language
English
Is part of
Journal of Thrombosis and Haemostasis (2015), Vol. 13, no. 6, p. 956-966
hdl
1887/102139
doi
10.1111/jth.12927