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Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2 mutation carriers
INTRODUCTION: Current attempts to identify genetic modifiers of BRCA1 and BRCA2 associated risk have focused on a candidate gene approach, based on knowledge of gene functions, or the development of large genome-wide association studies. In this study, we evaluated 24 SNPs tagged to 14 candidate gen...
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3046447/ https://www.ncbi.nlm.nih.gov/pubmed/21114847 http://dx.doi.org/10.1186/bcr2785 |