The AKT MES subtype was characterized by mutations in NF1 and RB1 and increased mRNA for the mesenchymal marker, MET, similar to the TCGA MES subgroup [10] , although these did not reach statistical significance.
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The AKT MES subtype was characterized by mutations in NF1 and RB1 and increased mRNA for the mesenchymal marker, MET, similar to the TCGA MES subgroup [10] , although these did not reach statistical significance.