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CRISPR/Cas9‐driven cancer modeling studies are based on the disruption of tumor suppressor genes by small insertions or deletions (indels) that lead to frame‐shift mutations. In addition, CRISPR/Cas9 is widely used to define the significance of cancer oncogenes and genetic dependencies in loss‐of‐function studies. However, how CRISPR/Cas9 influences gain‐of‐function oncogenic mutations is elusive...
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