Exome sequencing identifies MUTYH mutations in a family with colorectal cancer and an atypical phenotype
Autor(es) y otros:
Fecha de publicación:
2014
Versión del editor:
Citación:
Gut (2014); doi:10.1136/gutjnl-2014-307084
ISSN:
Identificador local:
20141702
Patrocinado por:
This work was funded by the Spanish Ministry of Economy and Competitiveness (State Secretariat for Research, Development and Innovation) (grants SAF2012-38885 and SAF2010-21165 to LV and XSP, Ramón y Cajal contract to LV, fellowship to FB, and RTICC networks RD12/0036/0031 and RD12/0036/0008); the Deutsche Krebshilfe (grant 110799 to GP); the Carlos III Health Institute (fellowship to NS); L’Oréal-UNESCO For Women in Science; the Scientific Foundation Asociación Española Contra el Cáncer; and the Government of Catalonia (grant 2009SGR290)
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