[E2] English Session 2
優秀English Session賞1

[E-010] Movement disorders and／or epileptic encephalopathies due to GNAO1 mutation：a four case report

Hiroya Nishida¹, Satoko Kumada¹, Kohei Hamanaka², Satoko Miyatake², Tadashi Kaname³, Yusuke Okuno⁴, Hideki Muramatsu⁵, Koichi Maruyama⁶, Mana Kurihara⁷, Takeshi Tsuji⁸, Kenji Inoue¹, Hideaki Mashimo¹, Atsuko Arisaka¹, Mitsumasa Fukuda¹, Naomichi Matsumoto² (1.Department of Neuropediatrics, Tokyo Metropolitan Neurological Hospital, Tokyo, Japan, 2.Department of Human Genetics, Yokohama City University Graduate School of Medicine, Kanagawa, Japan, 3.Department of Genome Medicine National Center for Child Health and Development, Tokyo, Japan, 4.Center for Advanced Medicine and Clinical Research, Nagoya University Hospital, Aichi, Japan, 5.Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan, 6.Department of Pediatric Neurology, Aichi Prefectural Colony Central Hospital, Aichi, Japan, 7.Department of Pediatrics, Kanagawa Rehabilitation Hospital, Kanagawa, Japan, 8.Department of Neuropediatrics, Okazaki City Hospital, Aichi, Japan)