Haematologica (Dec 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

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

DOI
https://doi.org/10.3324/haematol.2010.027177
Journal volume & issue
Vol. 95, no. 12

Abstract

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