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
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