We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleUncovering genomic causes of co-morbidity in epilepsy: gene-driven phenotypic characterization of rare microdeletions.AuthorsKasperavičiūtė D; Catarino CB; Chinthapalli K; Clayton LM; Thom M; Martinian L; Cohen H; Adalat S; Bockenhauer D; Pope SA; Lench N; Koltzenburg M; Duncan JS; Hammond P; Hennekam RC; Land JM; Sisodiya SMPublicationPloS one, 2011, Vol 6, Issue 8, pe23182ISSN1932-6203Publication typearticleDOI10.1371/journal.pone.0023182