We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleOhtahara syndrome in a family with an ARX protein truncation mutation (c.81C>G/p.Y27X).AuthorsFullston, Tod; Brueton, Louise; Willis, Tracey; Philip, Sunny; MacPherson, Lesley; Finnis, Merran; Gecz, Jozef; Morton, JennyPublicationEuropean Journal of Human Genetics, 2010, Vol 18, Issue 2, p157ISSN1018-4813Publication typearticleDOI10.1038/ejhg.2009.139