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Rare Variants in Known Susceptibility Loci and Their Contribution to Risk of Lung Cancer
BACKGROUND: Genome-wide association studies (GWAS) are widely used to map genomic regions contributing to lung cancer (LC) susceptibility but they typically do not identify the precise disease-causing genes/variants. To unveil the inherited causal LC variants, we performed focused exome sequencing a...
Gorde:
| Argitaratua izan da: | J Thorac Oncol |
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| Egile Nagusiak: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
2018
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6366341/ https://ncbi.nlm.nih.gov/pubmed/29981437 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jtho.2018.06.016 |
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