WiN Study Group: CLEC4M and STXBP5 gene variations contribute to von Willebrand factor level variation in von Willebrand disease.
SourceJournal of Thrombosis and Haemostasis, 13, (2015), pp. 956-966
Article / Letter to editor
Display more detailsDisplay less details
Paediatrics - OUD tm 2017
Journal of Thrombosis and Haemostasis
Upload full text
Use your RU credentials (u/z-number and password) to log in with SURFconext to upload a file for processing by the repository team.