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RUNX1 Mutations in the Leukemic Progression of Severe Congenital Neutropenia
Somatic RUNX1 mutations are found in approximately 10% of patients with de novo acute myeloid leukemia (AML), but are more common in secondary forms of myelodysplastic syndrome (MDS) or AML. Particularly, this applies to MDS/AML developing from certain types of leukemia-prone inherited bone marrow f...
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| Vydáno v: | Mol Cells |
|---|---|
| Hlavní autoři: | , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Korean Society for Molecular and Cellular Biology
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7057833/ https://ncbi.nlm.nih.gov/pubmed/32041395 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.14348/molcells.2020.0010 |
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