Ghezzi, Laura <br/><br/>
A 66-year-old patient with vanishing white matter disease due to the p.Ala87Val EIF2B3 mutation.  [electronic resource] 

 -  Neurology  Nov 2012 
 - 2077-8 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1526-632X 
<br/><br/><label>Standard No.: </label>10.1212/WNL.0b013e3182749edc  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aged<br/>Alanine--genetics<br/>Eukaryotic Initiation Factor-2B--genetics<br/>Female<br/>Humans<br/>Leukoencephalopathies--genetics<br/>Mutation--genetics<br/>Valine--genetics