We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleMutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency.AuthorsJaksch M; Ogilvie I; Yao J; Kortenhaus G; Bresser HG; Gerbitz KD; Shoubridge EAPublicationHuman molecular genetics, 2000, Vol 9, Issue 5, p795ISSN0964-6906Publication typearticleDOI10.1093/hmg/9.5.795