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

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

• Book ID: 116752115
• Publisher: Elsevier Science
• Year: 2011
• Tongue: English
• Weight: 57 KB
• Volume: 11
• Category: Article
• ISSN: 1567-7249
• DOI: 10.1016/j.mito.2011.03.017