Assessment of the Olfactory Function in Italian Patients with Type 3 von Willebrand Disease Caused by a Homozygous 253 Kb Deletion Involving VWF and TMEM16B/ANO2

Author:

Cenedese Valentina,Mezzavilla Massimo,Morgan Anna,Marino Renato,Ettorre Cosimo Pietro,Margaglione Maurizio,Gasparini Paolo,Menini Anna

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference41 articles.

1. New development in von Willebrand disease;G Castaman;Curr Opin Hematol,2013

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

3. The molecular basis of type 3 von Willebrand disease;AM Cumming;J Coag Dis.,2010

4. Atherosclerosis and von Willebrand factor. I. Prevalence of severe von Willebrand’s disease in western Europe and Israel;PM Mannucci;Br J Haematol,1984

5. von Willebrand factor: clinical features of inherited and acquired disorders;AL Bloom;Mayo Clin Proc,1991

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