Evaluation of the JAK2V617F Mutational Burden in Patients with Philadelphia Chromosome Negative Myeloproliferative Neoplasms: A Single-center Experience

The identification of the JAK2V617F mutation in several distinct myeloproliferative neoplasms (MPNs) raised the question how one single mutation incites expression of at least three different clinical phenotypes, i.e., polycythemia vera (PV), essential thrombocythemia (ET) and primary myelofibrosis...

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Detalles Bibliográficos
Autores principales: Popova-Labachevska, M, Panovska-Stavridis, I, Eftimov, A, Kapedanovska, Nestorovska A, Cevreska, L, Ivanovski, M, Ridova, N, Trajkova, S, Dimovski, AJ
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sciendo 2019
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6956630/
https://www.ncbi.nlm.nih.gov/pubmed/31942414
http://dx.doi.org/10.2478/bjmg-2019-0021

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6956630/
https://www.ncbi.nlm.nih.gov/pubmed/31942414
http://dx.doi.org/10.2478/bjmg-2019-0021

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