[O31] 遺伝・先天異常 3

[O31-1] Analysis of neuronal phenotypes in MECP2 duplication syndrome model and involvement of miR-199a in the pathophysiology

^○Yuichi Akaba^1,9, Satoru Takahashi¹, Yasunari Sakai², Yohei Hayashi³, Itaru Kushima^4,5, Daisuke Mori^5,6, Yuko Arioka^7,8, Norio Ozaki⁸, Keita Tsujimura⁹ (1.Department of Pediatrics, Asahikawa Medical University, Asahikawa, Hokkaido, Japan, 2.Department of Pediatrics, Kyushu University, Fukuoka, Japan, 3.iPS Cell Advanced Characterization and Development Team, RIKEN BioResource Research Center, Tsukuba, Ibaraki, Japan, 4.Medical Genomics Center, Nagoya University Hospital, Nagoya, Aichi, Japan, 5.Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan, 6.Brain and Mind Research Center, Nagoya University, Nagoya, Aichi, Japan, 7.Center for Advanced Medicine and Clinical Research, Nagoya University Hospital, Nagoya, Aichi, Japan, 8.Pathophysiology of Mental Disorders, Nagoya University, Nagoya, Aichi, Japan, 9.Group of Brain Function and Development, Nagoya University Neuroscience Institute of the Graduate School of Science, Nagoya, Aichi, Japan)