Gungor, O <br/><br/>
A rare mutation in EIF2B4 gene in an epileptic child with vanishing white matter disease: a case report.  [electronic resource] 

 -  Genetic counseling (Geneva, Switzerland)  2015 
 - 41-6 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1015-8146 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Epilepsy--genetics<br/>Eukaryotic Initiation Factor-2B--genetics<br/>Humans<br/>Infant<br/>Leukoencephalopathies--genetics<br/>Male<br/>Mutation