A novel FNDC3B::MECOM fusion gene accompanied with Der(5; 17)(p10; q10) in acute myelocytic leukemia
Author:
Funder
the Clinical Medicine + X Grant of the Affiliated Hospital of Qingdao University
Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s00277-024-05930-6.pdf
Reference5 articles.
1. Wang H-Y, McMahon C, Ali SM et al (2016) Novel FNDC3B and MECOM fusion and WT1 L378fs* 7 frameshift mutation in an acute myeloid leukaemia patient with cytomorphological and immunophenotypic features reminiscent of acute promyelocytic leukaemia. Br J Haematol 172(6):987–990 Published July 6, 2015
2. Menezes J, Makishima H, Gomez I et al (2013) CSF3R T618I co-occurs with mutations of splicing and epigenetic genes and with a new PIM3 truncated fusion gene in chronic neutrophilic leukemia. Blood cancer J 3:e158 Published November 8, 2013
3. Manabe M, Okita J, Tarakuwa T et al (2014) Der(5;17)(p10;q10) is a recurrent but rare whole-arm translocation in patients with hematological neoplasms: a report of three cases. Acta Haematol 132(2):134–139
4. Hong M, Hao S, Patel KP et al (2016) Whole-arm translocation of Der(5;17)(p10;q10) with concurrent TP53 mutations in acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS): a unique molecular-cytogenetic subgroup. Cancer Genet 209(5):205–214
5. Grob T, Al Hinai ASA, Sanders MA et al (2022) Molecular characterization of mutant TP53 acute myeloid leukemia and high-risk myelodysplastic syndrome. Blood 139(15):2347–2354
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