The V617F mutation of JAK2 is very uncommon in patients with thrombosis

Department of Hematology, Hospital de Sant Pau, Avda Padre Claret 167, Barcelona 08025, Spain Correspondence: Angel F. Remacha, Department of Hematology, Hospital de Sant Pau, Avda Padre Claret 167, Barcelona 08025, Spain. Phone: international +34.9.32919290. Fax: international +34.9.32919192. E-mai...

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Veröffentlicht in:Haematologica (Roma) 2007-02, Vol.92 (2), p.285-286
Hauptverfasser: Remacha, Angel F, Estivill, Camino, Sarda, M. Pilar, Mateo, Jose, Souto, Joan Carles, Canals, Carme, Nomdedeu, Josep, Fontcuberta, Jordi
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Sprache:eng
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Zusammenfassung:Department of Hematology, Hospital de Sant Pau, Avda Padre Claret 167, Barcelona 08025, Spain Correspondence: Angel F. Remacha, Department of Hematology, Hospital de Sant Pau, Avda Padre Claret 167, Barcelona 08025, Spain. Phone: international +34.9.32919290. Fax: international +34.9.32919192. E-mail: aremacha{at}hsp.santpau.es Given that many cases of thrombosis do not have a clear cause, a myeloproliferative disease could be involved. We investigated the V617F mutation of the JAK2 gene in 295 patients with thrombosis. Only one case was positive. Therefore, the study of this mutation is not necessary in all patients with idiopathic thrombosis. Key words: JAK2 mutation, idiopathic thrombosis.
ISSN:0390-6078
1592-8721
DOI:10.3324/haematol.10358