Lynch, C. J., Cawte, A. D., Millar, C. M., Rueda, D., & Lane, D. A. (2017). A common mechanism by which type 2A von Willebrand disease mutations enhance ADAMTS13 proteolysis revealed with a von Willebrand factor A2 domain FRET construct. PLoS One.
Citação norma ChicagoLynch, Christopher J., Adam D. Cawte, Carolyn M. Millar, David Rueda, and David A. Lane. "A Common Mechanism By Which Type 2A Von Willebrand Disease Mutations Enhance ADAMTS13 Proteolysis Revealed With a Von Willebrand Factor A2 Domain FRET Construct." PLoS One 2017.
Citação norma MLALynch, Christopher J., et al. "A Common Mechanism By Which Type 2A Von Willebrand Disease Mutations Enhance ADAMTS13 Proteolysis Revealed With a Von Willebrand Factor A2 Domain FRET Construct." PLoS One 2017.