Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleNovel POMGnT1 mutations define broader phenotypic spectrum of muscle–eye–brain disease.AuthorsHehr, Ute; Uyanik, Goekhan; Gross, Claudia; Walter, Maggie; Bohring, Axel; Cohen, Monika; Oehl-Jaschkowitz, Barbara; Bird, Lynne; Shamdeen, Ghiat; Bogdahn, Ulrich; Schuierer, Gerhard; Topaloglu, Haluk; Aigner, Ludwig; Lochmüller, Hanns; Winkler, JürgenPublicationNeurogenetics, 2007, Vol 8, Issue 4, p279ISSN1364-6745Publication typeArticleDOI10.1007/s10048-007-0096-y