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

Caporali, Leonardo

DGUOK recessive mutations in patients with CPEO, mitochondrial myopathy, parkinsonism and mtDNA deletions. [electronic resource] - Brain : a journal of neurology 01 2018 - e3 p. digital

Publication Type: Letter; Research Support, Non-U.S. Gov't; Comment

1460-2156

10.1093/brain/awx301 doi


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