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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...

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Xehetasun bibliografikoak
Argitaratua izan da:J Thorac Oncol
Egile Nagusiak: Liu, Yanhong, Lusk, Christine M., Cho, Michael H., Silverman, Edwin K., Qiao, Dandi, Zhang, Ruyang, Scheurer, Michael E., Kheradmand, Farrah, Wheeler, David A., Tsavachidis, Spiridon, Armstrong, Georgina, Zhu, Dakai, Wistuba, Ignacio I., Chow, Chi-Wan B., Behrens, Carmen, Pikielny, Claudio W., Neslund-Dudas, Christine, Pinney, Susan M., Anderson, Marshall, Kupert, Elena, Bailey-Wilson, Joan, Gaba, Colette, Mandal, Diptasri, You, Ming, de Andrade, Mariza, Yang, Ping, Field, John K., Liloglou, Triantafillos, Davies, Michael, Lissowska, Jolanta, Swiatkowska, Beata, Zaridze, David, Mukeriya, Anush, Janout, Vladimir, Holcatova, Ivana, Mates, Dana, Milosavljevic, Sasa, Scelo, Ghislaine, Brennan, Paul, McKay, James, Liu, Geoffrey, Hung, Rayjean J., Christiani, David C., Schwartz, Ann G., Amos, Christopher I, Spitz, Margaret R.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2018
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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