We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleFatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene.AuthorsPapadopoulou LC; Sue CM; Davidson MM; Tanji K; Nishino I; Sadlock JE; Krishna S; Walker W; Selby J; Glerum DM; Coster RV; Lyon G; Scalais E; Lebel R; Kaplan P; Shanske S; De Vivo DC; Bonilla E; Hirano M; DiMauro S; Schon EAPublicationNature genetics, 1999, Vol 23, Issue 3, p333ISSN1061-4036Publication typearticleDOI10.1038/15513