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APA Citation
Fernandez‐Mercado, M., Pellagatti, A., Di Genua, C., Larrayoz, M. J., Winkelmann, N., Aranaz, P., Burns, A., Schuh, A., Calasanz, M. J., Cross, N. C. P., & Boultwood, J. (n.d.). mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression. British journal of haematology, 163, 235–239. http://access.bl.uk/ark:/81055/vdc_100024542861.0x000047