S-EPMC11946544 - KMT2C/D mutations in newly diagnosed acute myeloid leukaemia: Clinical features, genetic co-occurrences and prognostic significance. - OmicsDI

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KMT2C/D mutations in newly diagnosed acute myeloid leukaemia: Clinical features, genetic co-occurrences and prognostic significance.

ABSTRACT:

SUBMITTER: Wang W

PROVIDER: S-EPMC11946544 | biostudies-literature | 2025 Apr

REPOSITORIES: biostudies-literature