Controversies about germline RUNX1 missense variants
Author:
Affiliation:
1. CHU Lille, Laboratory of Hematology, Lille, France;
2. INSERM, UMR-S 1172, Lille, France
Publisher
Informa UK Limited
Subject
Cancer Research,Oncology,Hematology
Link
https://www.tandfonline.com/doi/pdf/10.1080/10428194.2019.1675882
Reference16 articles.
1. Genomic analysis of a familial myelodysplasia/acute myeloid leukemia and inherited RUNX1 mutations without a pre-existing platelet disorder
2. Role of RUNX1 in hematological malignancies
3. Myelodysplastic syndromes and acute leukemia with genetic predispositions: a new challenge for hematologists
4. Germline RUNX1 Intragenic Deletion: Implications for Accurate Diagnosis of FPD/AML
5. RUNX1 meets MLL: epigenetic regulation of hematopoiesis by two leukemia genes
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2. Functional classification of RUNX1 variants in familial platelet disorder with associated myeloid malignancies;Leukemia;2021-03-10
3. Characterization of the Platelet Phenotype Caused by a Germline RUNX1 Variant in a CRISPR/Cas9-Generated Murine Model;Thrombosis and Haemostasis;2021-02-18
4. Germline RUNX1 mutations/deletions and genetic predisposition to hematological malignancies;Hématologie;2021-02
5. An analysis of the RUNX1p.(Leu56Ser) variant in a cohort of individuals with myeloid neoplasms; suggests it is a benign germline variant;Leukemia & Lymphoma;2020-12-21
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