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Highly Sensitive Detection of IDH2 Mutations in Acute Myeloid Leukemia
Background: Acute myeloid leukemia is a heterogeneous hematological disease, characterized by karyotypic and molecular alterations. Mutations in IDH2 have a role in diagnosis and as a minimal residue disease marker. Often the variant allele frequency during follow up is less than 20%, which represen...
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| Publicado no: | J Clin Med |
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| Main Authors: | , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7019902/ https://ncbi.nlm.nih.gov/pubmed/31963812 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/jcm9010271 |
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