Reply: DGUOK recessive mutations in patients with CPEO, mitochondrial myopathy, parkinsonism and mtDNA deletions

Research output: Contribution to journalLetter

Original languageEnglish
Pages (from-to)e4
JournalBrain
Volume141
Issue number1
DOIs
Publication statusPublished - Jan 1 2018

ASJC Scopus subject areas

  • Clinical Neurology

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