The new provisional WHO entity 'RUNX1 mutated AML' shows specific genetics but no prognostic influence of dysplasia
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu dopisy
PubMed
27211269
PubMed Central
PMC5056958
DOI
10.1038/leu.2016.150
PII: leu2016150
Knihovny.cz E-zdroje
- MeSH
- akutní myeloidní leukemie genetika patologie MeSH
- lidé MeSH
- prognóza MeSH
- protein PEBP2A2 genetika MeSH
- Světová zdravotnická organizace MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- dopisy MeSH
- Názvy látek
- protein PEBP2A2 MeSH
- RUNX1 protein, human MeSH Prohlížeč
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