Detection of SCN1A mutations in patients with severe myoclonic epilepsy in infancy by custom resequence array
, , , , oraz
10 cze 2013
O artykule
Data publikacji: 10 cze 2013
Zakres stron: 5 - 13
Otrzymano: 24 maj 2012
Przyjęty: 03 cze 2013
DOI: https://doi.org/10.21307/joepi-2015-0001
Słowa kluczowe
© 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