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. 2017 Mar;56(3):283–290. doi: 10.1165/rcmb.2016-0301PS

Figure 2.

Figure 2.

CRISPR/Cas9 delivery methods. Viral vectors using adeno-associated virus (AAV) and nonviral vectors using lipid nanoparticles are potentially effective methods for delivery of gene-editing tools into both airway and alveolar epithelial cells.