In contrast, the NRG1 SNVs cohort demonstrated numerically lower frequencies of KRAS (9.1%, P=0.19) and PIK3CA (13.6%, P>0.99) mutations compared with the NRG1 fusion cohort; however, these differences did not reach statistical significance.
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Analysis of clinical and genomic features in a Chinese cohort with <i>NRG1</i> variations: a retrospective study.
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