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10.3389/fnins.2023.1225875 Front

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5.6 CRISPR-Cas9 and genomic correction CRISPR-Cas9 enables precise genome editing and holds transformative potential for monogenic PD, particularly: Correction of LRRK2 G2019S , SNCA triplications, or PINK1 mutations

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Finally, the in vivo efficacy of these small-molecule-derived HBs was demonstrated through transplantation into DMN-induced acute liver failure NSI mice