[3P-725_3AS-17-04] Involvement of casein kinase 1 epsilon/delta (Csnk1e/d) in the pathogenesis of familial Parkinson’s disease caused by CHCHD2 gene mutations

^○Satoru Torii¹, Satoko Arakawa², Shigeto Sato³, Keiichi Ishikawa^3,4, Daisuke Taniguchi³, Hajime Sakurai⁵, Shinya Honda¹, Yuuichi Hiraoka^6,7, Masaya Ono⁸, Wado Akamatsu⁴, Nobutaka Hattori³, Shigeomi Shimizu¹ (1.Dept. of Pathol. Cell Biol., Med. Res. Inst., Tokyo Med. Dent. Univ., 2.Res. Core Cent., Tokyo Med. Dent. Univ., 3.Dept. of Neurol., Sch. of Med., Juntendo Univ., 4.Cent. for Gen. Reg. Med., Juntendo Univ., 5.Dept. of Mol. Biochem., Grad. Sch. of Life Sci., Univ. of Hyogo, 6.Lab. of Mol. Neuro., Med. Res. Inst., Tokyo Med. Dent. Univ., 7.Lab. of Gen. Edit. for Biomed. Res., Med. Res. Inst., Tokyo Med. Dent. Univ., 8.Dept. of Clin. Proteo., Nat. Can. Cent. Res. Inst.)