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. Haematologica; https://doi.org/10.3324/haematol.2025.287900 [Early view].