Casana P, Cabrera N, Haya S, Cid A, Aznar J. Von Willebrand’s disease: a novel mutation, P1824H and the incidence of R1205H defect among families with dominant quantitative von Willebrand factor deficiency. Haematologica [Internet]. 2006Aug.1 [cited 2026Nov.12];91(8):1130-3. Available from: https://haematologica.org/article/view/4106