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Discovery of rare coding variants in OGDHL and BRCA2 in relation to breast cancer risk in Chinese women
The missing heritability of breast cancer could be partially attributed to rare variants (MAF < 0.5%). To identify breast cancer-associated rare coding variants, we conducted whole-exome sequencing (~50×) in genomic DNA samples obtained from 831 breast cancer cases and 839 controls of Chinese fem...
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| Pubblicato in: | Int J Cancer |
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| Autori principali: | , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2019
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7453427/ https://ncbi.nlm.nih.gov/pubmed/31837001 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ijc.32825 |
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