[1E-140-52] Poster presentation (Advanced technology + Stem cells, Regeneration)

[1E-145] Induction of gigantic deletions for multi-exon skipping-based DMD therapy by the dual CRISPR-Cas3

*Yuto Kita¹, Yuya Okuzaki², Youichi Naoe¹, Akane Ichiki¹, Natsumi Okawa¹, Yusuke Kojima¹, Tomoji Mashimo³, Hidetoshi Sakurai¹, Akitsu Hotta¹ (1. Kyoto University, 2. Nagoya University, 3. The University of Tokyo)

Keywords:Genome editing, Duchenne muscular dystrophy, Gene therapy