Kasapkara, Çiğdem Seher <br/><br/>
A new NBIA patient from Turkey with homozygous C19ORF12 mutation.  [electronic resource] 

 -  Acta neurologica Belgica  Dec 2019 
 - 623-625 p.  digital 
<br/><br/> Publication Type: Case Reports; Letter 
<br/><br/><label>ISSN: </label>2240-2993 
<br/><br/><label>Standard No.: </label>10.1007/s13760-018-1026-5  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Homozygote<br/>Humans<br/>Iron Metabolism Disorders--genetics<br/>Mitochondrial Proteins--genetics<br/>Mutation<br/>Neuroaxonal Dystrophies--genetics<br/>Turkey