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Kerr, KM.; Dafni, U.; Schulze, K.; Thunnissen, E.; Bubendorf, L.; Hager, H.; Finn, S.... (2018). Prevalence and clinical association of gene mutations through multiplex mutation testing in patients with NSCLC: from the ETOP Lungscape Project. Annals of Oncology. 29(1):200-208. doi:10.1093/annonc/mdx629
Por favor, use este identificador para citar o enlazar este ítem: http://hdl.handle.net/10251/111248
Título: | Prevalence and clinical association of gene mutations through multiplex mutation testing in patients with NSCLC: from the ETOP Lungscape Project | |
Autor: | Kerr, K. M. Dafni, U. Schulze, K. Thunnissen, E. Bubendorf, L. Hager, H. Finn, S. Biernat, W. Vliegen, L. Losa, J. H. Marchetti, A. Cheney, R. Warth, A. Speel, E.-J. Jantus-Lewintre, Eloisa | |
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[EN] Background
Reported prevalence of driver gene mutations in non-small-cell lung cancer (NSCLC) is highly variable and clinical correlations are emerging. Using NSCLC biomaterial and clinical data from the European ...[+]
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Derechos de uso: | Cerrado | |
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Versión del editor: | http://dx.doi.org/10.1093/annonc/mdx629 | |
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