We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleSUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafnessAuthorsCarrozzo, R.; Dionisi-Vici, C.; Steuerwald, U.; Lucioli, S.; Deodato, F.; Di Giandomenico, S.; Bertini, E.; Franke, B.; Kluijtmans, L. A. J.; Meschini, M. C.; Rizzo, C.; Piemonte, F.; Rodenburg, R.; Santer, R.; Santorelli, F. M.; van Rooij, A.; Vermunt-de Koning, D.; Morava, E.; Wevers, R. A.PublicationBrain, 2007, Vol 130, Issue 3, p862ISSN0006-8950Publication typearticleDOI10.1093/brain/awl389