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Genetic risk variants in the CDKN2A/B, RTEL1 and EGFR genes are associated with somatic biomarkers in glioma
During the last years, genome wide association studies have discovered common germline genetic variants associated with specific glioma subtypes. We aimed to study the association between these germline risk variants and tumor phenotypes, including copy number aberrations and protein expression. A t...
Autores principales: | Ghasimi, Soma, Wibom, Carl, Dahlin, Anna M., Brännström, Thomas, Golovleva, Irina, Andersson, Ulrika, Melin, Beatrice |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4835517/ https://www.ncbi.nlm.nih.gov/pubmed/26839018 http://dx.doi.org/10.1007/s11060-016-2066-4 |
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