Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleSeven novel SCN1A mutations in Chinese patients with severe myoclonic epilepsy of infancy.AuthorsSun, Huihui; Yuehua Zhang; Jianmin Liang; Xiaoyan Liu; Xiuwei Ma; Jiong Qin; Yu Qi; Xiru WuAbstractA letter to the editor is presented on sodium channel gene (SCN1A) mutation in patients with severe myoclonic epilepsy of infancy.SubjectsLETTERS to the editor; EPILEPSYPublicationEpilepsia (Series 4), 2008, Vol 49, Issue 6, p1104ISSN0013-9580Publication typeLetterDOI10.1111/j.1528-1167.2008.01549_2.x