von Willebrand disease type 1 mutation p.Arg1379Cys and the variant p.Ala1377Val synergistically determine a 2M phenotype in four Italian patients
Pagliari, M. T., Baronciani, L., Stufano, F., Garcia-Oya, I., Cozzi, G., Franchi, F., Peyvandi, F.Language:
english
Journal:
Haemophilia
DOI:
10.1111/hae.13084
Date:
October, 2016
File:
PDF, 325 KB
english, 2016