Detection of SCN1A mutations in patients with severe myoclonic epilepsy in infancy by custom resequence array
Authors
Takayuki Sugawara
Department of Neuropsychiatry, Hirosaki University Graduate School of Medicine, Hirosaki, Japan
Research Institute of Bio-system Informatics, Tohoku Chemical Co., Ltd, Morioka, Japan
Shuichi Yoshida
Department of Integrated Human Sciences, Hamamatsu University School of Medicine, Hamamatsu, Japan
Naoko Onodera
Department of Neuropsychiatry, Hirosaki University Graduate School of Medicine, Hirosaki, Japan
Research Institute of Bio-system Informatics, Tohoku Chemical Co., Ltd, Morioka, Japan
Kazumaru Wada
Department of Disability and Health, Division of Health Sciences, Hirosaki University Graduate School of Health Sciences, Hirosaki, Japan
Shinichi Hirose
Department of Pediatrics, School of Medicine, Fukuoka University, Fukuoka, Japan
Sunao Kaneko
Department of Neuropsychiatry, Hirosaki University Graduate School of Medicine, Hirosaki, Japan
Language: English
Page range: 5 - 13
Submitted on: May 24, 2012
Accepted on: Jun 3, 2013
Published on: Jun 10, 2013
Published by: The Foundation of Epileptology
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year
Keywords:
Related subjects:
© 2013 Takayuki Sugawara, Shuichi Yoshida, Naoko Onodera, Kazumaru Wada, Shinichi Hirose, Sunao Kaneko, published by The Foundation of Epileptology
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.