Tanner, Stephan M <br/><br/>
Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns.  [electronic resource] 

 -  Orphanet journal of rare diseases  Aug 2012 
 - 56 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>10.1186/1750-1172-7-56  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Anemia, Megaloblastic<br/>Ethnicity--genetics<br/>Female<br/>Founder Effect<br/>Genetic Association Studies<br/>Genetic Heterogeneity<br/>Genetic Testing<br/>Humans<br/>Intrinsic Factor--genetics<br/>Malabsorption Syndromes--ethnology<br/>Male<br/>Membrane Proteins<br/>Mutation<br/>Proteins--genetics<br/>Proteinuria--ethnology<br/>Vitamin B 12--metabolism<br/>Vitamin B 12 Deficiency--ethnology