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Characterisation of the p.A1461D mutation causing von Willebrand disease type 2B with severe thrombocytopenia, circulating giant platelets, and defective α-granule secretion
Langer, F., Obser, T., Oyen, F., Spath, B., Holstein, K., Greinacher, A., White, J. G., Budde, U., Bokemeyer, C., Schneppenheim, R.Volume:
111
Language:
english
Journal:
Thrombosis and Haemostasis
DOI:
10.1160/TH13-06-0462
Date:
December, 2013
File:
PDF, 2.24 MB
english, 2013