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Sequence variants at the TERT- CLPTM1L locus associate with many cancer types
The common sequence variants that have recently been associated with cancer risk are particular to a single, or at most two, cancer types. Following up on our genome-wide scan of basal cell carcinoma(1), we identified rs401681(C) on chromosome 5p15.33 satisfying our threshold for genome-wide signifi...
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| Publicat a: | Nat Genet |
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| Autors principals: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2009
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4525478/ https://ncbi.nlm.nih.gov/pubmed/19151717 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ng.296 |
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