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Mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression.

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Title: Mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression.
Authors: Fernandez‐Mercado, Marta1, Pellagatti, Andrea1, Di Genua, Cristina1, Larrayoz, Maria Jose2, Winkelmann, Nils3, Aranaz, Paula2,3, Burns, Adam4, Schuh, Anna4, Calasanz, Maria Jose2, Cross, Nicholas C. P.3,5, Boultwood, Jacqueline1
Source: British Journal of Haematology. Oct2013, Vol. 163 Issue 2, p235-239. 5p. 2 Charts.
Database: Academic Search Ultimate
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