Genetic variation in the C-type lectin receptor CLEC4M in type 1 von Willebrand Disease patients
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Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference30 articles.
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1. Associations of multiple genetic variations with plasma levels of Von Willebrand Factor and clinical phenotype in Iranian patients with Von Willebrand disease type 1;Transfusion and Apheresis Science;2023-10
2. The contribution of the sinusoidal endothelial cell receptors CLEC4M, stabilin-2, and SCARA5 to VWF–FVIII clearance in thrombosis and hemostasis;Journal of Thrombosis and Haemostasis;2023-08
3. Hypercoagulability in COVID-19: A review of the potential mechanisms underlying clotting disorders;SAGE Open Medicine;2021-01
4. Common and Rare Variants in Genes Associated with von Willebrand Factor Level Variation: No Accumulation of Rare Variants in Swedish von Willebrand Disease Patients;TH Open;2020-10
5. The role of genetics in the pathogenesis and diagnosis of type 1 Von Willebrand disease;Current Opinion in Hematology;2019-09
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