Dravet syndrome: Patients with co-morbid SCN1A gene mutations and mitochondrial electron transport chain defects

✍ Scribed by Alexa K. Craig; Marcio Sotero de Menezes; Russell P. Saneto

• Book ID: 116880925
• Publisher: Elsevier Science
• Year: 2012
• Tongue: English
• Weight: 107 KB
• Volume: 21
• Category: Article
• ISSN: 1059-1311
• DOI: 10.1016/j.seizure.2011.08.010