[P-551] Gene therapy and genome editing therapy for type 2 rickets model rats using adenoviral vector

^○Satoko Kise¹, Tadashi Okada^2,3, Kaori Yasuda¹, Miyu Nishikawa¹, Shinnichi Ikushiro¹, Yoshiaki Kanemoto², Shigeaki Kato^2,3, Tomoko Nakanihi⁴, Izumu Saito⁴, Toshiyuki Sakaki¹ (1.Toyama Prefectural University, 2.TOKIWA Research Institute of Innovative Medicine, 3.IRYO SOSEI UNIVERSITY community medical center, 4.Juntendo University medicine)

キーテクノロジー：アデノウイルスベクター

遺伝子治療、アデノウイルスベクター、CRISPR-Cas9、くる病