Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleDGUOK recessive mutations in patients with CPEO, mitochondrial myopathy, parkinsonism and mtDNA deletions.AuthorsCaporali, Leonardo; Bello, Luca; Tagliavini, Francesca; Morgia, Chiara La; Maresca, Alessandra; Di Vito, Lidia; Liguori, Rocco; Valentino, Maria Lucia; Cecchin, Diego; Pegoraro, Elena; Carelli, Valerio; La Morgia, ChiaraSubjectsMITOCHONDRIAL myopathy; MITOCHONDRIAL DNA; GENETIC mutation; PARKINSONIAN disorders; RECESSIVE genesPublicationBrain: A Journal of Neurology, 2018, Vol 141, Issue 1, p1ISSN0006-8950Publication typeletterDOI10.1093/brain/awx301