Characterization of a novel FLI1 mutation in a family with thrombocytopenia and other congenital malformationsDaniele Ammeti(IRCCS Materno Infantile Burlo Garofolo), Stefania Bigoni(University of Ferrara)HaematologicaJune 5, 202510.3324/haematol.2024.287120Cited by 0SaveCiteExport RISWatch citationsRelated PapersGain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome|Genome Medicine|2022|22Additional file 2 of Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome|Open MIND|2022|0