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Viral and Non-Viral Systems to Deliver Gene Therapeutics to Clinical Targets

4 Jul 2024

Abstract excerpt

Clustered regularly interspersed short palindromic repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) technology has revolutionized the field of gene therapy as it has enabled precise genome editing with unprecedented accuracy and efficiency, paving the way for clinical applications to treat otherwise incurable genetic disorders. Typically, precise genome editing requires the delivery of multiple components to...

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PMID: 39000440
DOI: 10.3390/ijms25137333

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