Hanisch, Frank <br/><br/>
SANDO syndrome in a cohort of 107 patients with CPEO and mitochondrial DNA deletions.  [electronic resource] 

 -  Journal of neurology, neurosurgery, and psychiatry  Jun 2015 
 - 630-4 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1468-330X 
<br/><br/><label>Standard No.: </label>10.1136/jnnp-2013-306748  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Age of Onset<br/>Aged<br/>Biopsy<br/>Child<br/>Cohort Studies<br/>DNA Helicases--genetics<br/>DNA Polymerase gamma<br/>DNA, Mitochondrial--genetics<br/>DNA-Directed DNA Polymerase--genetics<br/>Dysarthria--epidemiology<br/>Female<br/>Gene Deletion<br/>Hereditary Sensory and Motor Neuropathy--epidemiology<br/>Humans<br/>Magnetic Resonance Imaging<br/>Male<br/>Middle Aged<br/>Mitochondrial Proteins--genetics<br/>Muscle, Skeletal--pathology<br/>Ophthalmoplegia--epidemiology<br/>Ophthalmoplegia, Chronic Progressive External--epidemiology<br/>Retrospective Studies<br/>Syndrome<br/>Young Adult