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Molecular heterogeneity and measurable residual disease of rare NPM1 mutations in acute myeloid leukemia: a nationwide experience from the GBMHM study group

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Authors and Affiliations



ND and SH (Huet) were responsible for designing the study. EF, AG, ND, and SH (Huet) conducted the literature search, extracted and analyzed the data, interpreted the results, wrote the manuscript and updated the reference lists. LF, CL, PFG, LM, LV, BS, and AMR contributed to the data extraction and analysis. MH, AP, CP, PS, SH, (Hayette) contributed to the data analysis and provided feedback on the manuscript.

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Correspondence to Sarah Huet.

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Fournier, E., Heiblig, M., Lespinasse, C. et al. Molecular heterogeneity and measurable residual disease of rare NPM1 mutations in acute myeloid leukemia: a nationwide experience from the GBMHM study group. Leukemia 36, 1390–1400 (2022).

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