The concomitant occurrence of JAK2V617F mutation and BCR/ABL transcript with phenotypic expression – an overlapping myeloproliferative disorder or two distinct diseases? - case report

The concomitant occurrence of JAK2617F mutation and BCR/ABL translocation is a rare event. It is unclear if this is a result of the clonal evolution or a separately emergence of two clones and if it could lead to the progression to a more aggressive phase of the disease. We present the case of a 61-...

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Detalles Bibliográficos
Autores principales: Ursuleac, I, Colita, AC, Adam, T, Jardan, C, Ilea, A, Coriu, D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Carol Davila University Press 2013
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3624642/
https://www.ncbi.nlm.nih.gov/pubmed/23599815

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3624642/
https://www.ncbi.nlm.nih.gov/pubmed/23599815

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