Pub. Date : 2016 Jul
PMID : 27148840
2 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
1 | Type 2B von Willebrand disease (VWD2B) is a rare, autosomal-dominant inherited bleeding disorder, characterized by an enhanced ristocetin-induced platelet aggregation in platelet-rich plasma and often with variable degree of thrombocytopenia and loss of high-molecular-weight multimers von Willebrand factor (VWF). | Ristocetin | von Willebrand factor | Homo sapiens |
2 | Type 2B von Willebrand disease (VWD2B) is a rare, autosomal-dominant inherited bleeding disorder, characterized by an enhanced ristocetin-induced platelet aggregation in platelet-rich plasma and often with variable degree of thrombocytopenia and loss of high-molecular-weight multimers von Willebrand factor (VWF). | Ristocetin | von Willebrand factor | Homo sapiens |