Roubertie, Agathe <br/><br/>
Neuroradiological findings expand the phenotype of OPA1-related mitochondrial dysfunction.  [electronic resource] 

 -  Journal of the neurological sciences  Feb 2015 
 - 154-60 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1878-5883 
<br/><br/><label>Standard No.: </label>10.1016/j.jns.2015.01.008  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Atrophy<br/>Brain--pathology<br/>Child<br/>Child, Preschool<br/>Female<br/>GTP Phosphohydrolases--genetics<br/>Hearing Loss--genetics<br/>Humans<br/>Magnetic Resonance Imaging<br/>Male<br/>Mitochondrial Diseases--genetics<br/>Motor Activity<br/>Neurologic Examination<br/>Optic Atrophy, Autosomal Dominant--genetics<br/>Young Adult