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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

作者：Giannini Silvia; Solimando Maria; Fierro Tiziana; Baronciani Luciano; Federici Augusto B; Gresele Paolo*
来源：Thrombosis and Haemostasis, 2011, 105(5): 921-924.
DOI：10.1160/TH10-08-0517
  • 出版日期2011-5

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更新时间：2018-02-09 13:50