Type 2N von Willebrand disease: Characterization and diagnostic difficulties

Author:

Casonato A.1ORCID,Galletta E.1,Sarolo L.1,Daidone V.1

Affiliation:

1. Department of Medicine; Hemorrhagic and Thrombotic Disorders Unit; University of Padua Medical School; Padua Italy

Funder

MURST

Publisher

Wiley

Subject

Genetics(clinical),Hematology,General Medicine

Reference32 articles.

1. Biochemistry and genetics of von Willebrand factor;Sadler;Annu Rev Biochem,1998

2. Von Willebrand factor mediates protection of FVIII from activated protein C-catalyzed inactivation;Fay;J Biol Chem,1991

3. Inactivation of human factor VIII by activated protein C. Cofactor activity of protein S and protective effect of von Willebrand factor;Koedam;J Clin Invest,1988

4. Stabilization of factor VIII in plasma by the von Willebrand factor. Studies on post-transfusion and dissociated factor VIII and in patients with von Willebrand ‘s disease;Weiss;J Clin Invest,1977

5. A major factor VIII binding domain resides within the amino terminal 272 amino acid residues of von Willebrand factor;Foster;J Biol Chem,1987

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