While KRAS mutant gains were more frequent in RNF43 MUT tumors, this did not reach statistical significance in our cohort (67% of RNF43 MUT tumors had KRAS mutant gains versus 30% in RNF43 WT , P = 0.2).
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Clinicogenomic landscape of pancreatic adenocarcinoma identifies KRAS mutant dosage as prognostic of overall survival.
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