Type 2B von Willebrand disease in seven individuals from three different families: phenotypic and genotypic characterization. [electronic resource]
- Thrombosis and haemostasis Jul 2007
- 251-4 p. digital
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
0340-6245
Adolescent Adult Dimerization Family Health Genotype Hemorrhage--etiology Humans Middle Aged Mutation, Missense Phenotype Thrombocytopenia--etiology von Willebrand Diseases--genetics von Willebrand Factor--genetics