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Prevalence and clinical association of gene mutations through multiplex mutation testing in patients with NSCLC: from the ETOP Lungscape Project

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Prevalence and clinical association of gene mutations through multiplex mutation testing in patients with NSCLC: from the ETOP Lungscape Project

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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

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Title: Prevalence and clinical association of gene mutations through multiplex mutation testing in patients with NSCLC: from the ETOP Lungscape Project
Author:
UPV Unit: Universitat Politècnica de València. Departamento de Biotecnología - Departament de Biotecnologia
Issued date:
Abstract:
[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 ...[+]
Subjects: Non-small-cell lung cancer , Multiplex mutation analysis , EGFR, KRAS, PIK3CA , Prognosis molecular staging
Copyrigths: Cerrado
Source:
Annals of Oncology. (issn: 0923-7534 )
DOI: 10.1093/annonc/mdx629
Publisher:
Oxford University Press
Publisher version: http://dx.doi.org/10.1093/annonc/mdx629
Type: Artículo

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