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Andrea Llanos-Ardaiz

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#gene editing Open access Sep 2026

Adeno-Associated Viral Vector (AAV)-Mediated In Vivo CRISPR-Cas9 Delivery.

This chapter detail a methodology using a rAAV vector carrying Staphylococcus aureus Cas9 (SaCas9) to target the murine Hao1 gene in liver parenchymal cells as a curative treatment for primary hyperoxaluria type 1 (PH1).

Andrea Llanos-Ardaiz, N. Zabaleta, Laura Torella et al. · 0 citations

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