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ASXL genes and RUNX1: an intimate connection?
In this issue of Blood, Micol et al report the discovery of mutations in the additional sex combs-like 2 (ASXL2) gene in about one-quarter of acute myeloid leukemia (AML) patients carrying the t(8;21) translocation.(1)
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
American Society of Hematology
2014
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| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4148754/ https://ncbi.nlm.nih.gov/pubmed/25170110 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2014-07-586073 |
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