Persistent URL of this record https://hdl.handle.net/1887/110289
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![Polymorphic variation within the VWF gene contributes to the failure to detect mutations in patients historically diagnosed with type 1 von Willebrand disease from the MCMDM-1VWD cohort](https://scholarlypublications.universiteitleiden.nl/sites/all/themes/scholarly/img/closed_access.png)
Polymorphic variation within the VWF gene contributes to the failure to detect mutations in patients historically diagnosed with type 1 von Willebrand disease from the MCMDM-1VWD cohort
- All authors
- Hampshire, D.J.; Burghel, G.J.; Goudemand, J.; Bouvet, L.C.S.; Eikenboom, J.C.J.; Schneppenheim, R.; Budde, U.; Peake, I.R.; Goodeve, A.C.; EU-VWD Grp; ZPMCB-VWD Study Grp
- Date
- 2010-12-31
- Journal
- Haematologica
- Volume
- 95
- Issue
- 12
- Pages
- 2163 - 2165