Impact of JAK2V617F Mutational Status on Phenotypic Features in Essential Thrombocythemia and Primary Myelofibrosis

OBJECTIVE: The JAK2V617F mutation is present in the majority of patients with essential thrombocythemia (ET) and primary myelofibrosis (PMF). The impact of this mutation on disease phenotype in ET and PMF is still a matter of discussion. This study aims to determine whether there are differences in...

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Bibliographische Detailangaben
Veröffentlicht in:Turk J Haematol
Hauptverfasser: Yönal, İpek, Dağlar-Aday, Aynur, Akadam-Teker, Başak, Yılmaz, Ceylan, Nalçacı, Meliha, Yavuz, Akif Selim, Sargın, Fatma Deniz
Format: Artigo
Sprache:Inglês
Veröffentlicht: Galenos Publishing 2016
Schlagworte:
Research Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5100738/
https://ncbi.nlm.nih.gov/pubmed/25913509
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4274/tjh.2014.0136
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