Detection of JAK2 exon 12 mutations in 15 patients with JAK2V617F negative polycythemia vera

To further characterize JAK2 exon 12 mutations, we performed molecular screening in 409 patients with polycythemia vera or unclear erythrocytosis with unmutated JAK2V617. The frequency of JAK2exon12 mutations was 10/63 (15.9%) in PV but only 5/346 (1.4%) in the erythrocytosis cases. Nine different m...

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Detalhes bibliográficos
Main Authors: Schnittger, Susanne, Bacher, Ulrike, Haferlach, Claudia, Geer, Thomas, Müller, Peter, Mittermüller, Johann, Petrides, Petro, Schlag, Rudolf, Sandner, Reiner, Selbach, Johannes, Slawik, Hans Rainer, Tessen, Hans Werner, Wehmeyer, Jürgen, Kern, Wolfgang, Haferlach, Torsten
Formato: Artigo
Idioma:Inglês
Publicado em: Ferrata Storti Foundation 2009
Assuntos:
Myeloproliferative Neoplasms
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2649350/
https://ncbi.nlm.nih.gov/pubmed/19252176
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3324/haematol.13223
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