| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 6015210 | Epilepsy Research | 2015 | 6 Pages |
Abstract
Mutations in SCN1A and SCN2A are a predisposing factor of AESD. Altered channel activity caused by these mutations may provoke seizures and excitotoxic brain damage.
Keywords
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Neurology
Authors
Makiko Saitoh, Atsushi Ishii, Yukiko Ihara, Ai Hoshino, Hiroshi Terashima, Masaya Kubota, Kenjiro Kikuchi, Gaku Yamanaka, Kaoru Amemiya, Shinichi Hirose, Masashi Mizuguchi,