P Casana, N Cabrera, S Haya, AR Cid, and JA Aznar. 2006. “Von Willebrand’s Disease: A Novel Mutation, P1824H and the Incidence of R1205H Defect Among Families With Dominant Quantitative Von Willebrand Factor Deficiency”. Haematologica 91 (8). Pavia, Italy, 1130-33. https://doi.org/10.3324/%x.