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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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Detalles Bibliográficos
Publicado en:Turk J Haematol
Main Authors: Yönal, İpek, Dağlar-Aday, Aynur, Akadam-Teker, Başak, Yılmaz, Ceylan, Nalçacı, Meliha, Yavuz, Akif Selim, Sargın, Fatma Deniz
Formato: Artigo
Idioma:Inglês
Publicado: Galenos Publishing 2016
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Acceso en liña: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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