DOI:
10.1055/s-00033990
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References
Casaña P, Martínez F, Haya S, Espinós C, Aznar JA.
Association of the 3467C>T mutation (T1156M) in the von Willebrand's factor gene with dominant type 1 von Willebrand's disease.
Ann Hematol 2001;
80 (07) 381-383
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