The Molecular Biology Society of Japan

[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 Horigane3,4, Jun Natsume2,5, Sayaka TakemotoKimura3,4, 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)

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