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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

Hampshire, Daniel J.; Burghel, George J.; Goudem, Jenny; Bouvet, Laura C.S.; Eikenboom, Jeroen C.J.; Schneppenheim, Reinhard; Budde, Ulrich; Peake, Ian R.; Goodeve, C.

Authors

George J. Burghel

Jenny Goudem

Laura C.S. Bouvet

Jeroen C.J. Eikenboom

Reinhard Schneppenheim

Ulrich Budde

Ian R. Peake

C. Goodeve



Citation

Hampshire, D. J., Burghel, G. J., Goudem, J., Bouvet, L. C., Eikenboom, J. C., Schneppenheim, R., Budde, U., Peake, I. R., & Goodeve, C. (2010). 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. Haematologica, 95(12), 2163-2165. https://doi.org/10.3324/haematol.2010.027177

Journal Article Type Letter
Publication Date Dec 1, 2010
Deposit Date May 24, 2022
Journal Haematologica
Print ISSN 0390-6078
Publisher Ferrata Storti Foundation
Peer Reviewed Peer Reviewed
Volume 95
Issue 12
Pages 2163-2165
DOI https://doi.org/10.3324/haematol.2010.027177
Public URL https://hull-repository.worktribe.com/output/3602032