Investigation of therapeutic modalities of G719X, an uncommon mutation in the EGFR gene in non-small

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Objective G719 X is the most frequently seen uncommon mutation of the epidermal growth factor receptor(EGFR) gene, which is a point mutation at exon 18 with three common subtypes, G719 A/G719 C/G719 S. This study explored the clinicopathological character
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