Title : Type 2B von Willebrand Disease: A Matter of Plasma Plus Platelet Abnormality.

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