Casana, P., Cabrera, N., Haya, S., Cid, A. and Aznar, J. (2006) “Von Willebrand’s disease: a novel mutation, P1824H and the incidence of R1205H defect among families with dominant quantitative von Willebrand factor deficiency”, Haematologica. Pavia, Italy, 91(8), pp. 1130-1133. Available at: https://haematologica.org/article/view/4106 (Accessed: 12November2026).