We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency.AuthorsOlsen RK; Olpin SE; Andresen BS; Miedzybrodzka ZH; Pourfarzam M; Merinero B; Frerman FE; Beresford MW; Dean JC; Cornelius N; Andersen O; Oldfors A; Holme E; Gregersen N; Turnbull DM; Morris AAPublicationBrain : a journal of neurology, 2007, Vol 130, Issue Pt 8, p2045ISSN1460-2156Publication typearticleDOI10.1093/brain/awm135