Characterization of rare germline variants in familial multiple myeloma
Jazyk angličtina Země Spojené státy americké Médium electronic
Typ dokumentu dopisy, práce podpořená grantem
Grantová podpora
11R/2019
José Carreras Leukämie-Stiftung (Deutsche José Carreras Leukämie-Stiftung)
PubMed
33583942
PubMed Central
PMC7882594
DOI
10.1038/s41408-021-00422-6
PII: 10.1038/s41408-021-00422-6
Knihovny.cz E-zdroje
- MeSH
- genetická predispozice k nemoci MeSH
- lidé MeSH
- missense mutace MeSH
- mnohočetný myelom genetika MeSH
- rodokmen MeSH
- zárodečné mutace * MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- dopisy MeSH
- práce podpořená grantem MeSH
Bioinformatics and Omics Data Analytics German Cancer Research Center Heidelberg Germany
Cedars Sinai Cancer Center Los Angeles CA USA
Department of Internal Medicine 5 University of Heidelberg Heidelberg Germany
Division of Cancer Epidemiology German Cancer Research Center Heidelberg Germany
Division of Molecular Genetic Epidemiology German Cancer Research Center Heidelberg Germany
Division of Pediatric Neurooncology German Cancer Research Center Heidelberg Germany
Faculty of Medicine and Biomedical Center in Pilsen Charles University Prague Pilsen Czech Republic
Hematology and Transfusion Medicine Department of Laboratory Medicine Lund University Lund Sweden
Hopp Children's Cancer Center Heidelberg Germany
Kempten Clinic Kempten Germany
National Center for Tumor Diseases Heidelberg Heidelberg Germany
University Medical Center Groningen University of Groningen Groningen The Netherlands
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Haplotype analysis identifies functional elements in monoclonal gammopathy of unknown significance
Investigation of Rare Non-Coding Variants in Familial Multiple Myeloma
Epidemiology, genetics and treatment of multiple myeloma and precursor diseases