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Publications by S. E. Lyons
Functional Analysis of a Type IIB Von Willebrand Disease Missense Mutation: Increased Binding of Large Von Willebrand Factor Multimers to Platelets.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
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Identification and Functional Analysis of a Novel Von Willebrand Factor Mutation in a Family With Type 2A Von Willebrand Disease
PLoS ONE
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Von Willebrand Disease Type 3
The Molecular Defect in Type IIB Von Willebrand Disease. Identification of Four Potential Missense Mutations Within the Putative GpIb Binding Domain.
Journal of Clinical Investigation
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Clearance of Von Willebrand Factor
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Mutations of Von Willebrand Factor Gene in Families With Von Willebrand Disease in the Aland Islands.
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Size Distribution Analysis of Von Willebrand Factor
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Von Willebrand Disease Lab Diagnosis
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Heterogeneous Phenotypes of Platelet and Plasma Von Willebrand Factor in Obligatory Heterozygotes for Severe Von Willebrand Disease
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Critical Von Willebrand Factor A1 Domain Residues Influence Type VI Collagen Binding
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