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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
 y 
Sunao Kaneko

Sunao Kaneko

Department of Neuropsychiatry, Hirosaki University Graduate School of MedicineHirosaki, Japan
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Kaneko, Sunao
  
10 jun 2013
Detection of SCN1A mutations in patients with severe myoclonic epilepsy in infancy by custom resequence array's Cover Image
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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.
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Inglés
Calendario de la edición:
2 veces al año
Temas de la revista:
Medicina, Medicina Clínica, Medicina Clínica, otros, Neurología, Farmacología, toxicología, Farmacia, Farmacia clínica
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