Trisomy 13 correlates with RUNX1 mutation and ... - Semantic Scholar
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Trisomy 13 correlates with RUNX1 mutation and ... - Semantic Scholar
3 gene encoding FLT3 (CD135), a class III receptor tyrosine kinase expressed in imma- ture hematopoietic cells and located on chromosome 13, is a good ...
Brief Report
Trisomy 13 correlates with RUNX1 mutation and increased FLT3 expression in AML-M0 patients Fernando P.G. Silva, Alexandra Lind, Geeske Brouwer-Mandema, Peter J.M. Valk, Micheline Giphart-Gassler
ABSTRACT From the Department of Toxicogenetics and Department of Hematology, Leiden University Medical Center, Leiden (FPGS, AL, GB-M and MG-P), The Netherlands and Department of Hematology, Erasmus University Medical Center, Rotterdam, The Netherlands (PJMV).
Of 52 AML-M0 patients studied, 16 presented a RUNX1 mutation (30.8 %) and 8 carried a trisomy 13 (15 %). We found a strong correlation between trisomy 13 and RUNX1 mutations, i.e, 7 out of 8 cases with trisomy 13 carried a mutation in RUNX1 (87.5 %, p
