## Abstract Decreased von Willebrand factor (VWF)βcleaving protease activity (<5%) has been implicated in patients with congenital thrombotic thrombocytopenic purpuraβhemolytic uremic syndrome (UpshawβSchulman syndrome) and associated with mutations within the __ADAMTS13__ gene. In this report, we
In vivo dissociation of factor vii (ahf) activity and factor viii-related antigen in von willebrand's disease
β Scribed by Eric Chun-Yet Lian; Daniel Deykin
- Publisher
- John Wiley and Sons
- Year
- 1976
- Tongue
- English
- Weight
- 407 KB
- Volume
- 1
- Category
- Article
- ISSN
- 0361-8609
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