[1P-465] Förster resonance energy transfer-based kinase mutation phenotyping reveals an aberrant facilitation of CaMKIIalpha activity in de novo mutations related to intellectual disability

^○Hajime Fujii¹, Hiroyuki Kidokoro², Yayoi Kondo¹, Masahiro Kawaguchi², Shinichiro Horigane^3,4, Jun Natsume^2,5, Sayaka TakemotoKimura^3,4, Haruhiko Bito¹ (1.Dept. of Neurochem, Grad. Sch. of Medicine, The Univ. of Tokyo, 2.Dept. of Pediatrics, Nagoya Univ. Grad. Sch. of Medicine, 3.Dept. of Neuroscience I, RIEM, Nagoya Univ., 4.Molecular/Cellular Neuroscience, Nagoya Univ. Grad. Sch. of Medicine, 5.Dept. of Developmental Disability Medicine, Nagoya Univ. Grad. Sch. of Medicine)