Calcoen B, Portier I, Pareyn I, Vandenbulcke A, Lehtinen A-E, Lassila R, Tersteeg C, Vanhoorelbeke K, De Meyer SF, Szanto T. A novel p.C1130S mutation in a Finnish family with a complex phenotype of von Willebrand disease. haematol [Internet]. 2020Sep.10 [cited 2025Dec.5];. Available from: https://haematologica.org/article/view/12236