High-throughput mutation profiling of primary and metastatic endometrial 
cancers identifies KRAS, FGFR2 and PIK3CA to be frequently mutated

Krakstad, Camilla; Birkeland, Even; Seidel, Danila; Kusonmano, Kanthida; Petersen, Kjell; Mjos, Siv; Hoivik, Erling A.; Wik, Elisabeth; Halle, Mari Kylleso; Oyan, Anne M.; Kalland, Karl-Henning; Werner, Henrica Maria Johanna; Trovik, Jone; Salvesen, Helga

doi:10.1371/journal.pone.0052795

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High-throughput mutation profiling of primary and metastatic endometrial cancers identifies KRAS, FGFR2 and PIK3CA to be frequently mutated

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Seidel, Danila
Funktionelle Krebsgenomforschung, Junior Research Groups, Max-Planck-Institut für neurologische Forschung, Managing Director: D. Yves von Cramon, Max Planck Institute for Metabolism Research, Managing Director: Jens Brüning, Max Planck Society;

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Krakstad, C., Birkeland, E., Seidel, D., Kusonmano, K., Petersen, K., Mjos, S., et al. (2012). High-throughput mutation profiling of primary and metastatic endometrial cancers identifies KRAS, FGFR2 and PIK3CA to be frequently mutated. PLoS ONE, 7(12): e52795. doi:10.1371/journal.pone.0052795.

Cite as: https://hdl.handle.net/11858/00-001M-0000-0026-D565-8