JAK2 V617F mutation in myelodysplastic syndrome, myelodysplastic syndrome/myeloproliferative neoplasm, unclassifiable, refractory anemia with ring sideroblasts with thrombocytosis, and acute myeloid leukemia

BACKGROUND: The JAK2 V617F mutation has been noted in the cases of polycythemia vera, essential thrombocythemia, and primary myelofibrosis patients. This mutation occurs less frequently in acute myeloid leukemia (AML) and other hematologic diseases, such as myelodysplastic syndrome (MDS); myelodyspl...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Jekarl, Dong Wook, Han, Sang Bong, Kim, Myungshin, Lim, Jihyang, Oh, Eun-Jee, Kim, Yonggoo, Kim, Hee-Je, Min, Woo-Sung, Han, Kyungja
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Korean Society of Hematology; Korean Society of Blood and Marrow Transplantation; Korean Society of Pediatric Hematology-Oncology; Korean Society on Thrombosis and Hemostasis 2010
Aiheet:
Original Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2983014/
https://ncbi.nlm.nih.gov/pubmed/21120162
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5045/kjh.2010.45.1.46
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