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Epilepsy Research|August 28, 2015
Missense mutations in sodium channel SCN1A and SCN2A predispose children to encephalopathy with severe febrile seizuresMakiko Saitoh, Atsushi Ishii, Yukiko Ihara, et al.
Brain & Development|August 27, 2014
Clinical and genetic features of acute encephalopathy in children taking theophyllineMakiko Saitoh, Mayu Shinohara, Atsushi Ishii, et al.
Science Advances|March 25, 2021
De novo ATP1A3 variants cause polymicrogyriaSatoko Miyatake, Mitsuhiro Kato, Takuma Kumamoto, et al.
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