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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.
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  Data: Mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression.
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  Data: <searchLink fieldCode="JN" term="%22British+Journal+of+Haematology%22">British Journal of Haematology</searchLink>. Oct2013, Vol. 163 Issue 2, p235-239. 5p. 2 Charts.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=90562354
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        Value: 10.1111/bjh.12491
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      – TitleFull: Mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression.
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              Text: Oct2013
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