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 - United States
doi 10.1172/jci115123
Full Text
Open PDFAbstract
Available in full text
Categories
Date
April 1, 1991
Authors
Publisher
American Society for Clinical Investigation