Whole-exome sequencing analysis of NSCLC reveals the pathogenic missense variants from cancer-associated genes.
Resource URI: https://dblp.l3s.de/d2r/resource/publications/journals/cbm/KumarBHVSGYZD22
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Whole-exome sequencing analysis of NSCLC reveals the pathogenic missense variants from cancer-associated genes.
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Whole-exome sequencing analysis of NSCLC reveals the pathogenic missense variants from cancer-associated genes.
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