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, p298ISSN1531-8249Publication typeResearchDOI10.1002/ana.23620