Home » Publications » DGUOK recessive mutations in patients with CPEO, mitochondrial myopathy, parkinsonism and mtDNA deletions
Caporali L., Bello L., Tagliavini F., La Morgia C., Maresca A., Di Vito L., Liguori R., Valentino M.L., Cecchin D., Pegoraro E., Carelli V.
Brain, Volume 141 Issue 1 Pages e3 (2018)
Links
DOI: https://doi.org/10.1093/brain/awx301
PMID: 29228108