NANOTECHNOLOGY-ENABLED NON-VIRAL DELIVERY SYSTEMS FOR CRISPR/CAS9 GENE THERAPY: CURRENT PROGRESS AND TRANSLATIONAL CHALLENGES
CRISPR/Cas9 has become a versatile platform for programmable genome editing and has generated substantial interest as a therapeutic modality for inherited and acquired diseases. However, clinical translation depends not only on editing specificity but also on safe and efficient delivery of the Cas9 nuclease and guide R...