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)

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