克拉斯
等位基因
生物
遗传学
癌症研究
医学
突变
计算生物学
癌症
生物信息学
危险分层
作者
Marco Meazza Prina,Laura Mezquita
标识
DOI:10.1158/1078-0432.ccr-26-2135
摘要
A recent article provides the largest characterization to date of KRAS Q61-mutant NSCLC. The findings reveal clinically relevant differences between Q61 alleles and highlight the importance of interpreting KRAS mutations within their genomic context. As RAS-directed therapies evolve, understanding this heterogeneity becomes increasingly relevant for patient stratification and therapeutic development.
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