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Rare occurrence of DNMT3A mutations in myelodysplastic syndromes
Gene mutations and epigenetic changes have been shown to play significant roles in the pathogenesis of myelodysplastic syndromes. Recently, mutations in DNMT3A were identified in 22.1% of patients with acute myeloid leukemia. In this study, we analyzed the frequency and clinical impact of DNMT3A mut...
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| Main Authors: | , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Ferrata Storti Foundation
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3232272/ https://ncbi.nlm.nih.gov/pubmed/21880636 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3324/haematol.2011.045559 |
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