Mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression. - Fernandez‐Mercado, Marta; Pellagatti, Andrea; Di Genua, Cristina; Larrayoz, Maria Jose; Winkelmann, Nils; Aranaz, Paula; Burns, Adam; Schuh, Anna; Calasanz, Maria Jose; Cross, Nicholas C. P.; Boultwood, Jacqueline (British Journal of Haematology, 2013)