Type 2B von Willebrand's disease due to Val1316Met mutation. Heterogeneity in the same sibship
- Rendal, E.
- Penas, N.
- Larrabeiti, B.
- Pérez, A.
- Vale, A.
- López-Fernández, M.
- Batlle, J.
ISSN: 0939-5555
Year of publication: 2001
Volume: 80
Issue: 6
Pages: 354-360
Type: Article