Beech, Cameron M <br/><br/>
Ancient founder mutation is responsible for Imerslund-Gräsbeck Syndrome among diverse ethnicities.  [electronic resource] 

 -  Orphanet journal of rare diseases  Nov 2011 
 - 74 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural 
<br/><br/><label>ISSN: </label>1750-1172 
<br/><br/><label>Standard No.: </label>10.1186/1750-1172-6-74  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Age Factors<br/>Anemia, Megaloblastic<br/>Arabs--genetics<br/>Asian People--genetics<br/>Ethnicity--genetics<br/>Female<br/>Founder Effect<br/>Genetics, Population<br/>Humans<br/>Jews--genetics<br/>Malabsorption Syndromes--ethnology<br/>Male<br/>Membrane Proteins<br/>Middle East<br/>Mutation<br/>Proteins--genetics<br/>Proteinuria--ethnology<br/>Vitamin B 12 Deficiency--ethnology