The E592K variant of SF3B1 creates unique RNA missplicing and associates with high-risk MDS without ring sideroblasts
SF3B1的E592K变体造成独特的RNA剪接错误,并与无环状铁粒幼细胞的高危MDS相关。
期刊:Blood Advances
影响因子:7.1
doi:10.1182/bloodadvances.2023011260
Choi, In Young; Ling, Jonathan P; Zhang, Jian; Helmenstine, Eric; Walter, Wencke; Tsakiroglou, Panagiotis; Bergman, Riley E; Philippe, Céline; Manley, James L; Rouault-Pierre, Kevin; Li, Bing; Wiseman, Daniel H; Batta, Kiran; Ouseph, Madhu; Bernard, Elsa; Dubner, Benjamin; Li, Xiao; Haferlach, Torsten; Koget, Anna; Fazal, Salman; Jain, Tania; Gocke, Christopher D; DeZern, Amy E; Dalton, William Brian