Concomitant JAK2 V617F mutation and rare e1a2 BCR-ABL1 transcript isoform in a patient with myeloproliferative neoplasm

Author:

Soriani SilviaORCID,Lauricella Calogero,Frungillo Niccolò,De Troia Beatrice Boido,Motta Valentina,Cesana Clara,Guido Valentina,De Canal Gabriella,De Paoli ElenaORCID,Veronese Silvio,Bonoldi Emanuela,Romitti LorenzaORCID

Publisher

Elsevier BV

Subject

General Medicine

Reference15 articles.

1. Frequency of rare BCR-ABL1 fusion transcripts in chronic myeloid leukemia patients;Arun;Int. J. Lab Hematol.,2017

2. Concurrent JAK2-positive myeloproliferative disorder and chronic myelogenous leukemia: a novel entity? A case report with review of the literature;Bader;J. Investig. Med. High Impact. Case Rep.,2019

3. JAK2-V617F mutation and Philadelphia positive chronic myeloid leukemia;Campiotti;Leuk. Res.,2009

4. De Roeck L., et al. Coexisting driver mutations in MPN: clinical and molecular characteristics of a series of 11 patients. Hematology. Dec;23(10):785–792.

5. Clinical and prognostic significance of e1a2 BCR-ABL1 transcript subtype in chronic myeloid leukemia;Gong;Blood Cancer J.,2017

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