Barely Significant
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Exome and genome sequencing of nasopharynx cancer identifies NF-κB pathway activating mutations.

Nat Commun · 2017 · PMC5253631 · PMID 28098136

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Additional genes which displayed recurrent mutations in our data set but did not reach statistical significance ( q <0.1) included the NF-κB pathway member NLRC5 , which was mutated in six cases (4.8%) ( Fig. 3a ).

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