Article
Acquired von Willebrand syndrome type 2A in a JAK2-positive essential thrombocythaemia-affected member of a large von Willebrand disease family with a novel autosomal dominant A1716P mutation.
Thrombosis and haemostasis - 1 May 2011
Giannini S, Solimando M, Fierro T, Baronciani L, Federici A B, Gresele P
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