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JAK2(V617F) Mutation Is Not Associated with Thrombosis in Behcet Syndrome
Ar, M. Cem; Hatemi, Gulen; Ekizoglu, Seda; Bilgen, Hulya; Sacli, Sevgi; Buyru, A. Nur; Yazici, Hasan (SAGE PUBLICATIONS INC, 2012)The Janus kinase 2(V617F) (JAK2(V617F)) mutation is an acquired genetic defect that is considered to enhance thrombosis in Philadelphia chromosome-negative myeloproliferative neoplasms (MPNs). Thrombosis is also a well-defined ...