P Casana, N Cabrera, S Haya, AR Cid, JA Aznar. Von Willebrand’s disease: a novel mutation, P1824H and the incidence of R1205H defect among families with dominant quantitative von Willebrand factor deficiency. haematol [Internet]. 2006Aug.1 [cited 2024Nov.22];91(8):1130-3. Available from: https://haematologica.org/article/view/4106