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A common mechanism by which type 2A von Willebrand disease mutations enhance ADAMTS13 proteolysis revealed with a von Willebrand factor A2 domain FRET construct
- Christopher J. Lynch,
- Adam D. Cawte,
- Carolyn M. Millar,
- David Rueda,
- David A. Lane
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- Published: November 29, 2017
- https://doi.org/10.1371/journal.pone.0188405