Associated Papers
Detection of SF3B1 p.Lys700Glu Mutation by PNA-PCR Clamping in Myelodysplastic Syndromes and Myeloproliferative Neoplasms.
Petiti J et al.
Journal of Clinical Medicine, 2022
The K666N mutation in SF3B1 is associated with increased progression of MDS and distinct RNA splicing.
Dalton WB et al.
Blood Advances, 2020
Somatic SF3B1 mutations in myelodysplastic syndrome with ring sideroblasts and chronic lymphocytic leukaemia.
Foy A et al.
Journal of Clinical Pathology, 2019
Somatic SF3B1 mutation in myelodysplasia with ring sideroblasts.
Papaemmanuil E et al.
The New England Journal of Medicine, 2011
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