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...

Cijeli opis

Spremljeno u:
Bibliografski detalji
Glavni autori: 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
Format: Artigo
Jezik:Inglês
Izdano: Ferrata Storti Foundation 2009
Teme:
Myeloproliferative Neoplasms
Online pristup: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
Oznake: Dodaj oznaku
Bez oznaka, Budi prvi tko označuje ovaj zapis!

Similar Items