Tanner, Stephan M <br/><br/>
Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor gene.  [electronic resource] 

 -  Proceedings of the National Academy of Sciences of the United States of America  Mar 2005 
 - 4130-3 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>0027-8424 
<br/><br/><label>Standard No.: </label>10.1073/pnas.0500517102  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 11<br/>Female<br/>Humans<br/>Intrinsic Factor--genetics<br/>Male<br/>Mutation<br/>Pedigree<br/>Vitamin B 12--metabolism<br/>Vitamin B 12 Deficiency--genetics