Single and multiple point NRAS mutations in acute myeloid leukemia: a study of 327 well molecularly characterized patients
Leukemia & lymphoma.
2022 Dec ;
63 (13) :
3237-3240.
[epub] 20220901
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
Persistent link
https://www.medvik.cz/link/pmid36047997
- MeSH
- Leukemia, Myeloid, Acute * diagnosis genetics MeSH
- Point Mutation MeSH
- GTP Phosphohydrolases genetics MeSH
- Humans MeSH
- Membrane Proteins genetics MeSH
- Mutation MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- GTP Phosphohydrolases MeSH
- Membrane Proteins MeSH
- NRAS protein, human MeSH Browser
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
References provided by Crossref.org
