Lanean...
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...
Gorde:
| Argitaratua izan da: | Mol Cells |
|---|---|
| Egile Nagusiak: | , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Korean Society for Molecular and Cellular Biology
2020
|
| Gaiak: | |
| Sarrera elektronikoa: | 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 |
| Etiketak: |
Etiketa erantsi
Etiketarik gabe, Izan zaitez lehena erregistro honi etiketa jartzen!
|