Tanner, Stephan M <br/><br/>
Genetically heterogeneous selective intestinal malabsorption of vitamin B12: founder effects, consanguinity, and high clinical awareness explain aggregations in Scandinavia and the Middle East.  [electronic resource] 

 -  Human mutation  Apr 2004 
 - 327-33 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>1098-1004 
<br/><br/><label>Standard No.: </label>10.1002/humu.20014  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Anemia, Megaloblastic--genetics<br/>Consanguinity<br/>DNA Mutational Analysis<br/>Female<br/>Founder Effect<br/>Haplotypes<br/>Humans<br/>Intestinal Absorption<br/>Male<br/>Membrane Proteins<br/>Middle East<br/>Mutation<br/>Pedigree<br/>Proteins--genetics<br/>Receptors, Cell Surface--genetics<br/>Scandinavian and Nordic Countries<br/>Vitamin B 12 Deficiency--diagnosis