Katipoğlu, Nagehan <br/><br/>
Infantile-onset thiamine responsive megaloblastic anemia syndrome with SLC19A2 mutation: a case report.  [electronic resource] 

 -  Archivos argentinos de pediatria  06 2017 
 - e153-e156 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1668-3501 
<br/><br/><label>Standard No.: </label>10.5546/aap.2017.eng.e153  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Anemia, Megaloblastic--genetics<br/>Diabetes Mellitus--genetics<br/>Female<br/>Hearing Loss, Sensorineural--genetics<br/>Humans<br/>Infant<br/>Membrane Transport Proteins--genetics<br/>Mutation<br/>Thiamine Deficiency--congenital