Densupsoontorn, Narumon <br/><br/>
Imerslund-Gräsbeck syndrome: new mutation in amnionless.  [electronic resource] 

 -  Pediatrics international : official journal of the Japan Pediatric Society  Jun 2012 
 - e19-21 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1442-200X 
<br/><br/><label>Standard No.: </label>10.1111/j.1442-200X.2011.03482.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Anemia, Megaloblastic<br/>Child, Preschool<br/>Humans<br/>Malabsorption Syndromes--genetics<br/>Male<br/>Membrane Proteins<br/>Mutation<br/>Proteins--genetics<br/>Proteinuria--genetics<br/>Vitamin B 12 Deficiency--genetics