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Precision medicine in heritable cancer: when somatic tumour testing and germline mutations meet
Cancer is among the leading causes of death and disfigurement worldwide with an estimated global incidence of 14 million and ~8.2 million cancer-related deaths per annum. An estimated 5–10% of all cancers are hereditary, meaning a single gene mutation contributed to development of the cancer. In oth...
Zapisane w:
| Wydane w: | NPJ Genom Med |
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| Główni autorzy: | , |
| Format: | Artigo |
| Język: | Inglês |
| Wydane: |
Nature Publishing Group
2016
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| Hasła przedmiotowe: | |
| Dostęp online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5685292/ https://ncbi.nlm.nih.gov/pubmed/29263804 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/npjgenmed.2015.6 |
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