دورية أكاديمية
Dravet syndrome: Patients with co-morbid SCN1A gene mutations and mitochondrial electron transport chain defects
| العنوان: | Dravet syndrome: Patients with co-morbid SCN1A gene mutations and mitochondrial electron transport chain defects |
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| المؤلفون: | Craig, Alexa K., de Menezes, Marcio Sotero, Saneto, Russell P. |
| المصدر: | In Seizure: European Journal of Epilepsy January 2012 21(1):17-20 |
| قاعدة البيانات: | ScienceDirect |
Full Text via ClinicalKey 
Full Text Finder | تدمد: | 10591311 |
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| DOI: | 10.1016/j.seizure.2011.08.010 |