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A genome wide SNP genotyping study in the Tunisian population: specific reporting on a subset of common breast cancer risk loci
BACKGROUND: Breast cancer is the most common cancer in women worldwide. Around 50% of breast cancer familial risk has been so far explained by known susceptibility alleles with variable levels of risk and prevalence. The vast majority of these breast cancer associated variations reported to date are...
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| 出版年: | BMC Cancer |
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| 主要な著者: | , , , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2018
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6310952/ https://ncbi.nlm.nih.gov/pubmed/30594178 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12885-018-5133-8 |
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