SF3B1 mutations and heme synthesis One of the most interesting findings resulting from the discovery of spliceosomal gene mutations was an unexpected and highly significant association between SF3B1 mutations and MDS subtypes with ringed sideroblasts ( Malcovati et al. 2015 ).
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Spliceosomal gene mutations in myelodysplasia: molecular links to clonal abnormalities of hematopoiesis.
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