Detection of SCN1A mutations in patients with severe myoclonic epilepsy in infancy by custom resequence array

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Open Access

|Jun 2013

Authors

Department of Neuropsychiatry, Hirosaki University Graduate School of Medicine, Hirosaki, Japan

Research Institute of Bio-system Informatics, Tohoku Chemical Co., Ltd, Morioka, Japan

Department of Integrated Human Sciences, Hamamatsu University School of Medicine, Hamamatsu, Japan

Department of Neuropsychiatry, Hirosaki University Graduate School of Medicine, Hirosaki, Japan

Research Institute of Bio-system Informatics, Tohoku Chemical Co., Ltd, Morioka, Japan

Department of Disability and Health, Division of Health Sciences, Hirosaki University Graduate School of Health Sciences, Hirosaki, Japan

Department of Pediatrics, School of Medicine, Fukuoka University, Fukuoka, Japan

Department of Neuropsychiatry, Hirosaki University Graduate School of Medicine, Hirosaki, Japan

DOI: https://doi.org/10.21307/joepi-2015-0001 | Journal eISSN: 2299-9728 | Journal ISSN: 2300-0147

Language: English

Page range: 5 - 13

Submitted on: May 24, 2012

Accepted on: Jun 3, 2013

Published on: Jun 10, 2013

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.