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Expanding cancer predisposition genes with ultra-rare cancer-exclusive human variations
It is estimated that up to 10% of cancer incidents are attributed to inherited genetic alterations. Despite extensive research, there are still gaps in our understanding of genetic predisposition to cancer. It was theorized that ultra-rare variants partially account for the missing heritable compone...
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| Vydáno v: | Sci Rep |
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| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Nature Publishing Group UK
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7418036/ https://ncbi.nlm.nih.gov/pubmed/32778766 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-020-70494-0 |
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