A novel p.C1130S mutation in a Finnish family with a complex phenotype of von Willebrand disease
Authors
- Tímea Szántó (ORCID: https://orcid.org/0000-0001-7006-6564)
- Aline Vandenbulcke (ORCID: https://orcid.org/0000-0001-7642-0616)
- Karen Vanhoorelbeke (ORCID: https://orcid.org/0000-0003-2288-8277)
- Anna‐Elina Lehtinen
- Bas Calcoen (ORCID: https://orcid.org/0000-0002-9095-9607)
- Claudia Tersteeg (ORCID: https://orcid.org/0000-0002-6380-6349)
- Irina Portier (ORCID: https://orcid.org/0000-0003-1993-9723)
- Riitta Lassila (ORCID: https://orcid.org/0000-0002-1911-3094)
- Simon F. De Meyer (ORCID: https://orcid.org/0000-0002-1807-5882)
- Inge Pareyn (ORCID: https://orcid.org/0000-0003-0602-0929)
Institutions
- University of Helsinki (FI)
- Helsinki University Hospital (FI)
- Thrombosis Research Institute (GB)
Funders
- Fonds Wetenschappelijk Onderzoek
- Vlaamse regering