CSF3R T618I is a highly prevalent and specific mutation in chronic neutrophilic leukemia - PubMed

Runx1 repression by histone deacetylation is critical for Setbp1-induced mouse myeloid leukemia development.

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International Consensus Classification of Myeloid Neoplasms and Acute Leukemias: integrating morphologic, clinical, and genomic data.

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Prognostic significance of SETBP1 mutations in myelodysplastic syndromes, chronic myelomonocytic leukemia, and chronic neutrophilic leukemia: A meta-analysis.

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B-lymphoblastic leukemia arising in a patient with chronic neutrophilic leukemia.

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Evaluation of a father and son with atypical chronic myeloid leukemia with SETBP1 mutations and a review of the literature.

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