PP2.7 – 2032 Benign familial infantile epilepsy due to PRRT2 gene mutation without paroxysmal kinesigenic dyskinesia

✍ Scribed by Maras, H; Kara, B; Yalcin, EU; Iseri, SU; Ozbek, U

• Book ID: 123504619
• Publisher: Elsevier Science
• Year: 2013
• Tongue: English
• Weight: 65 KB
• Volume: 17
• Category: Article
• ISSN: 1090-3798
• DOI: 10.1016/S1090-3798(13)70117-X