Presentation Information
[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
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