An analysis of the RUNX1p.(Leu56Ser) variant in a cohort of individuals with myeloid neoplasms; suggests it is a benign germline variant
Author:
Affiliation:
1. OncoGenomics, University College London, UK
Publisher
Informa UK Limited
Subject
Cancer Research,Oncology,Hematology
Link
https://www.tandfonline.com/doi/pdf/10.1080/10428194.2020.1861272
Reference15 articles.
1. Controversies about germline RUNX1 missense variants
2. RUNX1 meets MLL: epigenetic regulation of hematopoiesis by two leukemia genes
3. The ability of MLL to bind RUNX1 and methylate H3K4 at PU.1 regulatory regions is impaired by MDS/AML-associated RUNX1/AML1 mutations
4. Pre-Donor Evaluation of an HLA Matched Sibling Identifies a Novel Inherited RUNX1 Mutation Encoding a Missense Mutation Found Outside of the RUNT Domain in Familial Platelet Disorder
5. Genomic analysis of a familial myelodysplasia/acute myeloid leukemia and inherited RUNX1 mutations without a pre-existing platelet disorder
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