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Blood, Vol. 113, Issue 22, 5583-5587, May 28, 2009 This Article Abstract Full Text Services Email this article to a friend Alert me to new issues of the journal Rights and Permissions Citing Articles Citing Articles via CrossRef High frequency of RUNX1 biallelic alteration in acute myeloid leukemia secondary to familial platelet disorder Blood Preudhomme et al. 113: 5583 Supplemental materials for: Preudhomme et al Files in this Data Supplement: Table S1. Primer sequences used for RUNX1 mutations screening (PDF, 38.1 KB) Figure S1. Structure of RUNX1 protein and location of mutations identified in this study (JPG, 227 KB) - Position numbering is based on the Swiss-Prot protein accession number Q01196-1 and corresponds to RUNX1 isoform 1b. Abbreviations: RHD, Runt homology domain; TAD, transactivation domain, CBF: core binding factor. This Article Abstract Full Text Services Email this article to a friend Alert me to new issues of the journal Rights and Permissions Citing Articles Citing Articles via CrossRef

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