Title: SCN2A mutation associated with neonatal epilepsy, late-onset episodic ataxia, myoclonus, and pain.

Authors: Y Liao, A-K Anttonen, E Liukkonen, E Gaily, S Maljevic, S Schubert, A Bellan-Koch, S Petrou, V E Ahonen, H Lerche, A-E Lehesjoki

Journal, date & volume: Neurology, 2010 Oct 19 , 75, 1454-8

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/20956790

Abstract