Article
Human iPSCs-based modeling unveils chromatin remodeling induced by SETBP1 mutation as a potential initiating factor in GATA2 deficiency
2024-09-04
Abstract excerpt
<title>Abstract</title> <p>Patients with GATA2 deficiency are predisposed to developing myelodysplastic syndrome (MDS), which can progress to acute myeloid leukemia (AML). This progression is often associated with the acquisition of additional cytogenetic and somatic alterations. Mutations in SETBP1 and ASXL1 genes are frequently observed in pediatric GATA2 patients, but their roles in disease progression remain...
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Identifiers and source
- Literature Corpus work
- 4014df2b-9544-58ff-9c30-499ce352c876
- DOI
- 10.21203/rs.3.rs-4984522/v1
