Absence of the JAK2 V617F mutation in patients with arterial thrombosis without overt myeloproliferative disease

2008-08-26

Additional Metadata
Keywords	Janus kinase 2, adult, artery thrombosis, article, blood clotting disorder, brain ischemia, cerebrovascular accident, clinical feature, female, gene mutation, heart muscle ischemia, hospital admission, human, major clinical study, male, myeloproliferative disorder, priority journal, thrombocyte count, transient ischemic attack
Persistent URL	doi.org/10.1111/j.1538-7836.2008.03081.x, hdl.handle.net/1765/15975
Journal	Journal of Thrombosis and Haemostasis
Organisation	Erasmus MC: University Medical Center Rotterdam
Citation APA Style AAA Style APA Style Cell Style Chicago Style Harvard Style IEEE Style MLA Style Nature Style Vancouver Style American-Institute-of-Physics Style Council-of-Science-Editors Style BibTex Format Endnote Format RIS Format CSL Format DOIs only Format	Smalberg, J., de Maat, M., & Leebeek, F. (2008). Absence of the JAK2 V617F mutation in patients with arterial thrombosis without overt myeloproliferative disease. Journal of Thrombosis and Haemostasis, 6(9), 1606–1607. doi:10.1111/j.1538-7836.2008.03081.x

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