Küçükçongar, A <br/><br/>
A case with rare type of congenital disorder of glycosylation: PGM1-CDG.  [electronic resource] 

 -  Genetic counseling (Geneva, Switzerland)  2015 
 - 87-90 p.  digital 
<br/><br/> Publication Type: Case Reports; Letter 
<br/><br/><label>ISSN: </label>1015-8146 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Female<br/>Glycogen Storage Disease--diagnosis<br/>Humans<br/>Infant