Calcoen, Bas, Irina Portier, Inge Pareyn, Aline Vandenbulcke, Anna-Elina Lehtinen, Riitta Lassila, Claudia Tersteeg, Karen Vanhoorelbeke, Simon F. De Meyer, and Timea Szanto. 2020. “A Novel p.C1130S Mutation in a Finnish Family With a Complex Phenotype of Von Willebrand Disease”. Haematologica, September. Pavia, Italy. https://doi.org/10.3324/haematol.2025.287900.