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A type 2B von Willebrand disease mutation (Ile546 to Val) associated with an unusual phenotype

Federici AB, Mannucci PM, Stabile F, Canciani MT, Di Rocco N, Miyata S, Ware J, Ruggeri ZM. A type 2B von Willebrand disease mutation (Ile546 to Val) associated with an unusual phenotype. Throm Haemost. 1997; 78:1132 - 1137.


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