Strange bedfellows: NPM1 mutations in acute promyelocytic leukemia
Author:
Publisher
Elsevier BV
Subject
Oncology,Hematology,General Medicine
Reference10 articles.
1. Clinicopathological significance of common genetic alterations in patients with acute promyelocytic leukemia;Nath;Hematol Oncol Stem Cell Ther,2020
2. Acute promyelocytic leukemia: update on the mechanisms of leukemogenesis, resistance and on innovative treatment strategies;Noguera;Cancers,2019
3. Nucleophosmin1 mutations in acute myeloid leukemia;Zarka;Genes,2020
4. NPM1 mutations and cytoplasmic nucleophosmin are mutually exclusive of recurrent genetic abnormalities: a comparative analysis of 2562 patients with acute myeloid leukemia;Falini;Haematologica,2008
5. Comprehensive mutational analysis of primary and relapse acute promyelocytic leukemia;Madan;Leukemia,2016
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1. Treatment of a Patient with Acute Promyelocytic Leukemia with Multiple Isolated Relapses in the Central Nervous System: A Case Report and Mini-Review of the Literature;Case Reports in Hematology;2024-05-03
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