SF3B1 mutation identifies a distinct subset of myelodysplastic syndrome with ring sideroblasts

Overview of attention for article published in Blood, May 2015

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SF3B1 mutation identifies a distinct subset of myelodysplastic syndrome. This article and commentary helps define this new subtype of with discussions on therapy. Really helpful as we do more and more molecular next-gen sequencing #MDS #camoldx #mdssm ht

28 Jul 2020

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SF3B1 mutation identifies a distinct subset of MDS w/ ring sideroblasts [2015] Malcovati et al. @BloodJournal https://t.co/06AYDB0Yi1 #mdssm

30 Aug 2019

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RT @mtmdphd: SF3B1 mutation identifies a distinct subset of MDS w/ ring sideroblasts [2015] Malcovati et al. @BloodJournal https://t.co/06A…

17 Jul 2017

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RT @mtmdphd: SF3B1 mutation identifies a distinct subset of MDS w/ ring sideroblasts [2015] Malcovati et al. @BloodJournal https://t.co/06A…

17 Jul 2017

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