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Sequencing a mouse acute promyelocytic leukemia genome reveals genetic events relevant for disease progression
Acute promyelocytic leukemia (APL) is a subtype of acute myeloid leukemia (AML). It is characterized by the t(15;17)(q22;q11.2) chromosomal translocation that creates the promyelocytic leukemia–retinoic acid receptor α (PML-RARA) fusion oncogene. Although this fusion oncogene is known to initiate AP...
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| Autors principals: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
American Society for Clinical Investigation
2011
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3069786/ https://ncbi.nlm.nih.gov/pubmed/21436584 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI45284 |
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