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Diagnostic and therapeutic pitfalls in NPM1-mutated AML: notes from the field
Mutations of Nucleophosmin (NPM1) are the most common genetic abnormalities in adult acute myeloid leukaemia (AML), accounting for about 30% of cases. NPM1-mutated AML has been recognized as distinct entity in the 2017 World Health Organization (WHO) classification of lympho-haematopoietic neoplasms...
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| Publicat a: | Leukemia |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Nature Publishing Group UK
2021
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8056374/ https://ncbi.nlm.nih.gov/pubmed/33879827 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41375-021-01222-4 |
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