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. Haematologica 2006;91(8):1130-1133; https://doi.org/10.3324/%x.