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Using germline variants to estimate glioma and subtype risks
BACKGROUND: Twenty-five single nucleotide polymorphisms (SNPs) are associated with adult diffuse glioma risk. We hypothesized that the inclusion of these 25 SNPs with age at diagnosis and sex could estimate risk of glioma as well as identify glioma subtypes. METHODS: Case-control design and multinom...
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| Publicado no: | Neuro Oncol |
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| Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6422428/ https://ncbi.nlm.nih.gov/pubmed/30624711 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/neuonc/noz009 |
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