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

Wenting Wang; Miao Yang; Xue Zhang; Jiayuan Chen; Shaowei Qiu; Bingcheng Liu; Yingchang Mi; Jianxiang Wang; Hui Wei

doi:10.1002/ctm2.70284

Clinical and Translational Medicine ›› 2025, Vol. 15 ›› Issue (4) : e70284 DOI: 10.1002/ctm2.70284

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

Wenting Wang ¹^,²
, Miao Yang ¹^,²
, Xue Zhang ¹^,²
, Jiayuan Chen ¹^,²
, Shaowei Qiu ¹^,²
, Bingcheng Liu ¹^,²
, Yingchang Mi ¹^,²
, Jianxiang Wang ¹^,²
, Hui Wei ¹^,²

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Wenting Wang, Miao Yang, Xue Zhang, Jiayuan Chen, Shaowei Qiu, Bingcheng Liu, Yingchang Mi, Jianxiang Wang, Hui Wei. KMT2C/D mutations in newly diagnosed acute myeloid leukaemia: Clinical features, genetic co-occurrences and prognostic significance. Clinical and Translational Medicine, 2025, 15(4): e70284 DOI:10.1002/ctm2.70284

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2025 The Author(s). Clinical and Translational Medicine published by John Wiley & Sons Australia, Ltd on behalf of Shanghai Institute of Clinical Bioinformatics.