Monsuur, Alienke J <br/><br/>
Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defect.  [electronic resource] 

 -  Nature genetics  Dec 2005 
 - 1341-4 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1061-4036 
<br/><br/><label>Standard No.: </label>10.1038/ng1680  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Celiac Disease--genetics<br/>Female<br/>Genetic Predisposition to Disease<br/>Haplotypes<br/>Humans<br/>Intestine, Small--physiopathology<br/>Introns--genetics<br/>Male<br/>Molecular Sequence Data<br/>Myosins--genetics<br/>Polymorphism, Single Nucleotide