DOI:
10.1055/s-00000077
Seminars in Thrombosis and Hemostasis
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References
Pagliari MT, Baronciani L, Stufano F. et al.
von Willebrand disease type 1 mutation p.Arg1379Cys and the variant p.Ala1377Val synergistically determine a 2M phenotype in four Italian patients.
Haemophilia 2016;
22 (06) e502-e511
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