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

Brain. 2018 Jan 1;141(1):e4. doi: 10.1093/brain/awx302.

Authors

Dario Ronchi¹, Daniela Piga¹, Stefano Lamberti¹, Monica Sciacco², Stefania Corti¹, Maurizio Moggio², Nereo Bresolin¹, Giacomo Pietro Comi¹

Affiliations

¹ Dino Ferrari Centre, Neuroscience Section, Department of Pathophysiology and Transplantation (DEPT), University of Milan, Neurology Unit, IRCCS Foundation Ca' Granda Ospedale Maggiore Policlinico, 20122 Milan, Italy.
² Neuromuscular and Rare Disease Unit, Department of Neuroscience, Fondazione IRCCS Ca' Granda Ospedale Policlinico Milano, Italy.

PMID: 29228135
DOI: 10.1093/brain/awx302

No abstract available

Publication types

Letter
Research Support, Non-U.S. Gov't
Comment

MeSH terms

Adult
DNA, Mitochondrial / genetics
High-Throughput Nucleotide Sequencing
Humans
Mitochondrial Myopathies*
Mutation
Ophthalmoplegia, Chronic Progressive External / genetics*
Parkinsonian Disorders*

Substances

DNA, Mitochondrial