Caporali, Leonardo <br/><br/>
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 
<br/><br/> Publication Type: Letter; Research Support, Non-U.S. Gov't; Comment 
<br/><br/><label>ISSN: </label>1460-2156 
<br/><br/><label>Standard No.: </label>10.1093/brain/awx301  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>DNA, Mitochondrial--genetics<br/>High-Throughput Nucleotide Sequencing<br/>Humans<br/>Mitochondrial Myopathies<br/>Mutation<br/>Ophthalmoplegia, Chronic Progressive External--genetics<br/>Parkinsonian Disorders