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Germline copy number variations are associated with breast cancer risk and prognosis
Breast cancer is one of the most common cancers among women, and susceptibility is explained by genetic, lifestyle and environmental components. Copy Number Variants (CNVs) are structural DNA variations that contribute to diverse phenotypes via gene-dosage effects or cis-regulation. In this study, w...
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| 發表在: | Sci Rep |
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| Main Authors: | , , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Nature Publishing Group UK
2017
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5677082/ https://ncbi.nlm.nih.gov/pubmed/29116104 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-017-14799-7 |
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