This commentary discusses unanswered questions about splicing factor mutations in blood cancers, suggesting new therapeutic strategies.
Summary: Mutations in genes encoding RNA splicing factors are common in patients with myeloid malignancies and chronic lymphocytic leukemia. In this commentary, we discuss key unanswered questions on the causal role of these mutations in blood cancers and precursor conditions as well as efforts to develop therapies targeting these high-frequency neomorphic mutations.
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Maron et al. (2026) studied this question.
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