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[In addition to the germline RUNX1 mutation, we identified a second RUNX1 alteration in 6 AML cases (acquired point mutations in 4 cases and duplication of the altered RUNX1 allele associated with acquired trisomy 21 in 2 other cases).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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