Detection of SCN1A mutations in patients with severe myoclonic epilepsy in infancy by custom resequence array
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10 jun 2013
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Publicado en línea: 10 jun 2013
Páginas: 5 - 13
Recibido: 24 may 2012
Aceptado: 03 jun 2013
DOI: https://doi.org/10.21307/joepi-2015-0001
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© 2013 Takayuki Sugawara et al., published by Sciendo
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
Sugawara, Takayuki
Department of Neuropsychiatry, Hirosaki University Graduate School of MedicineHirosaki, Japan
Research Institute of Bio-system Informatics, Tohoku Chemical Co., LtdMorioka, Japan
Yoshida, Shuichi
Department of Integrated Human Sciences, Hamamatsu University School of MedicineHamamatsu, Japan
Onodera, Naoko
Department of Neuropsychiatry, Hirosaki University Graduate School of MedicineHirosaki, Japan
Research Institute of Bio-system Informatics, Tohoku Chemical Co., LtdMorioka, Japan
Wada, Kazumaru
Department of Disability and Health, Division of Health Sciences, Hirosaki University Graduate School of Health SciencesHirosaki, Japan
Hirose, Shinichi
Department of Pediatrics, School of Medicine, Fukuoka UniversityFukuoka, Japan
Kaneko, Sunao
Department of Neuropsychiatry, Hirosaki University Graduate School of MedicineHirosaki, Japan