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Rare coding variants and breast cancer risk: Evaluation of susceptibility loci identified in genome-wide association studies
BACKGROUND: To date, common genetic variants in ~70 loci have been identified for breast cancer via genome-wide association studies (GWAS). It is unknown whether rare variants in these loci are also associated with breast cancer risk. METHODS: We investigated rare missense/nonsense variants with min...
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| Autors principals: | , , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2014
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3976694/ https://ncbi.nlm.nih.gov/pubmed/24470074 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1158/1055-9965.EPI-13-1043 |
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