A novel RUNX1 mutation with ANKRD26 dysregulation is related to thrombocytopenia in a sporadic form of myelodysplastic syndrome - Ferrari, Silvia; Regazzo, Daniela; Omenetto, Elisabetta; Scaroni, Carla; Semenzato, Gianpietro; Fabris, Fabrizio; Vianello, Fabrizio (Aging clinical and experimental research, 2021)
Keywords: Anemia; Core Binding Factor Alpha 2 Subunit - genetics; Erythrocytes; Genetic Predisposition to Disease; Geriatrics/Gerontology; Humans; Intercellular Signaling Peptides and Proteins; Leukemia; Medicine; Medicine & Public Health; Mutation; Myelodysplastic Syndromes; Short Communication; Thrombocytopenia; Thrombocytopenia; Platelets; Myelodysplastic syndromes; ANKRD26; RUNX1