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

Takayuki Sugawara

Takayuki Sugawara

  • Department of Neuropsychiatry, Hirosaki University Graduate School of MedicineHirosaki, Japan
  • Research Institute of Bio-system Informatics, Tohoku Chemical Co., LtdMorioka, Japan
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Sugawara, Takayuki
, 
Shuichi Yoshida

Shuichi Yoshida

Department of Integrated Human Sciences, Hamamatsu University School of MedicineHamamatsu, Japan
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Yoshida, Shuichi
, 
Naoko Onodera

Naoko Onodera

  • Department of Neuropsychiatry, Hirosaki University Graduate School of MedicineHirosaki, Japan
  • Research Institute of Bio-system Informatics, Tohoku Chemical Co., LtdMorioka, Japan
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Onodera, Naoko
, 
Kazumaru Wada

Kazumaru Wada

Department of Disability and Health, Division of Health Sciences, Hirosaki University Graduate School of Health SciencesHirosaki, Japan
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Wada, Kazumaru
, 
Shinichi Hirose

Shinichi Hirose

Department of Pediatrics, School of Medicine, Fukuoka UniversityFukuoka, Japan
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Hirose, Shinichi
 and 
Sunao Kaneko

Sunao Kaneko

Department of Neuropsychiatry, Hirosaki University Graduate School of MedicineHirosaki, Japan
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Kaneko, Sunao
  
Jun 10, 2013
Detection of SCN1A mutations in patients with severe myoclonic epilepsy in infancy by custom resequence array's Cover Image
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Published Online: Jun 10, 2013
Page range: 5 - 13
Received: May 24, 2012
Accepted: Jun 03, 2013
DOI: https://doi.org/10.21307/joepi-2015-0001
Keywords
© 2013 Takayuki Sugawara et al., published by Sciendo
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
Language:
English
Publication timeframe:
2 times per year
Journal Subjects:
Medicine, Clinical Medicine, Clinical Medicine, other, Neurology, Pharmacology, Toxicology, Pharmacy, Clinical Pharmacy
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