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. 2020 Oct 22;9(11):2337. doi: 10.3390/cells9112337

Figure 1.

Figure 1

(A) Distribution of mutations detected in NSCLC (n = 56) patients cfDNA. (B) Two MassARRAY plots from patient P04 showing an EGFR exon19 deletion and a p.T790M resistance causing mutation.