L Hilbert, AB Federici, L Baronciani, S Dallagiovanna, C Mazurier. A new candidate mutation, G1629R, in a patient with type 2A von Willebrand’s disease: basic mechanisms and clinical implications. haematol [Internet]. 2004Sep.1 [cited 2024Aug.31];89(9):1128-33. Available from: https://haematologica.org/article/view/3225