Özgün, Nezir <br/><br/>
A rare cause of epileptic encephalopathy: a beta-propeller protein associated neurodegeneration case with a new mutation and literature review.  [electronic resource] 

 -  The Turkish journal of pediatrics  2020 
 - 109-113 p.  digital 
<br/><br/> Publication Type: Case Reports; Review; Journal Article 
<br/><br/><label>ISSN: </label>2791-6421 
<br/><br/><label>Standard No.: </label>10.24953/turkjped.2020.01.015  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Carrier Proteins--genetics<br/>Electroencephalography<br/>Epilepsy--genetics<br/>Female<br/>Humans<br/>Infant<br/>Magnetic Resonance Imaging<br/>Mutation