Associated Papers
Genome-Wide Analysis Identifies MEN1 and MAX Mutations and a Neuroendocrine-Like Molecular Heterogeneity in Quadruple WT GIST.
Pantaleo MA et al.
Molecular Cancer Research : Mcr, 2017
Somatic loss of function mutations in neurofibromin 1 and MYC associated factor X genes identified by exome-wide sequencing in a wild-type GIST case.
Belinsky MG et al.
Bmc Cancer, 2015
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