Article
Rapid discrimination of the phenotypic variants of von Willebrand disease.
Blood - 19 May 2016
Roberts Jonathan C, Morateck Patti A, Christopherson Pamela A, Yan Ke, Hoffmann Raymond G, Gill Joan Cox, Montgomery Robert R
Abstract excerpt
Approximately 20% to 25% of patients with von Willebrand disease (VWD) have a qualitative defect of the von Willebrand factor (VWF) protein activities. Variant VWD typically is classified as type 1C, 2A, 2B, 2M, or 2N depending on the VWF activity defect. Traditionally, diagnosis has relied on multiple clinical laboratory assays to assign VWD phenotype. We developed an enzyme-linked immunosorbent assay (ELISA) to...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
