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Adenovirus-Mediated Somatic Genome Editing of Pten by CRISPR/Cas9 in Mouse Liver in Spite of Cas9-Specific Immune Responses.
Cas9-mediated allelic exchange repairs compound heterozygous recessive mutations in mice.
AAV5 delivery of CRISPR-Cas9 supports effective genome editing in mouse lung airway.
Self-inactivating, all-in-one AAV vectors for precision Cas9 genome editing via homology-directed repair in vivo.