We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleWhole exome sequencing identifies KCNQ2 mutations in Ohtahara syndrome.AuthorsSaitsu, Hirotomo; Kato, Mitsuhiro; Koide, Ayaka; Goto, Tomohide; Fujita, Takako; Nishiyama, Kiyomi; Tsurusaki, Yoshinori; Doi, Hiroshi; Miyake, Noriko; Hayasaka, Kiyoshi; Matsumoto, NaomichiPublicationAnnals of Neurology, 2012, Vol 72, Issue 2, p298ISSN0364-5134Publication typearticleDOI10.1002/ana.23620