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3 research outputs found
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
Author
Bouvet L.C.S.
Budde U.
+9 more
Burghel G.J.
Eikenboom J.C.J.
EU-VWD Grp
Goodeve A.C.
Goudemand J.
Hampshire D.J.
Peake I.R.
Schneppenheim R.
ZPMCB-VWD Study Grp
Publication venue
Ferrata Storti Foundation
Publication date
01/12/2010
Field of study
No full text
Thrombosis and Hemostasi
Repository@Hull - Worktribe
Crossref
PubMed Central
Leiden University Scholary Publications
Copy number variation is a significant contributor to type 1 VWD pathogenesis in the EU MCMDM-1VWD cohort
Author
Al-Buhairan A.M.
Bloomer L.D.
+12 more
Budde U.
Cartwright A.
Eikenboom J.C.J.
EU-VWD Grp
Goodeve A.C.
Habart D.
Hampshire D.J.
Hill F.G.H.
Peake I.R.
Rodeghiero F.
Vijzelaar R.N.C.P.
ZPMCB-VWD Study Grp
Publication venue
Publication date
31/07/2011
Field of study
No full text
Copy number variation is a significant contributor to type 1 VWD pathogenesis in the EU MCMDM-1VWD cohort
Author
Al-Buhairan A.M.
Bloomer L.D.
+12 more
Budde U.
Cartwright A.
Eikenboom J.C.J.
EU-VWD Grp
Goodeve A.C.
Habart D.
Hampshire D.J.
Hill F.G.H.
Peake I.R.
Rodeghiero F.
Vijzelaar R.N.C.P.
ZPMCB-VWD Study Grp
Publication venue
Publication date
31/07/2011
Field of study
No full text
Thrombosis and Hemostasi
Leiden University Scholary Publications