Institutional members access full text with Ovid®

Share this article on:

Arg578Gln mutations in the von Willebrand factor gene in three unrelated cases of type IIB von Willebrand disease

Piao Y. C.; Lavergne, J. M.; Boyer-Neumann, C.; Schandelong, A.; Alessi, M. C.; Meyer, D.
Blood Coagulation & Fibrinolysis: October 1993 - Volume 4 - Issue 5 - ppg 787-789
Mutation Report: PDF Only