Stefan Lethagen (Former)
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- 2018
-
Mark
Genetic variation in the C-type lectin receptor CLEC4M in type 1 von Willebrand Disease patients
(
- Contribution to journal › Article
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Mark
Genetic Variation in the Syntaxin-Binding Protein STXBP5 in Type 1 von Willebrand Disease Patients
(
- Contribution to journal › Article
- 2017
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Mark
European retrospective study of real-life haemophilia treatment
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- Contribution to journal › Article
- 2011
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Mark
A large deletion identified in a Swedish family with type 1 VWD
(
- Contribution to journal › Letter
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Mark
Variation in the VWF Gene in Swedish Patients with Type 1 von Willebrand Disease.
(
- Contribution to journal › Article