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Single and multiple point NRAS mutations in acute myeloid leukemia: a study of 327 well molecularly characterized patients
A. Durinikova, A. Folta, F. Pardy, J. Svaton, M. Drncova, B. Weinbergerova, P. Cetkovsky, Z. Racil, P. Jindra, T. Szotkowski, P. Zak, J. Mayer, I. Jeziskova
Leukemia & lymphoma.
2022 ;
63 (13) :
3237-3240.
[pub] 20220901
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
Perzistentní odkaz
https://www.medvik.cz/link/bmc22032451
- MeSH
- akutní myeloidní leukemie * diagnóza genetika MeSH
- bodová mutace MeSH
- GTP-fosfohydrolasy genetika MeSH
- lidé MeSH
- membránové proteiny genetika MeSH
- mutace MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Central European Institute of Technology Masaryk University Brno Czech Republic
Department of Hemato Oncology University Hospital Olomouc Olomouc Czech Republic
Department of Hematology and Oncology University Hospital Pilsen Pilsen Czech Republic
Department of Internal Medicine Hematology and Oncology University Hospital Brno Brno Czech Republic
Institute of Hematology and Blood Transfusion Prague Czech Republic
Citace poskytuje Crossref.org
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