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, 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.Volume:
95
Language:
english
Journal:
Haematologica
DOI:
10.3324/haematol.2010.027177
Date:
December, 2010
File:
PDF, 1.03 MB
english, 2010