Hunt, K A <br/><br/>
Lack of association of MYO9B genetic variants with coeliac disease in a British cohort.  [electronic resource] 

 -  Gut  Jul 2006 
 - 969-72 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0017-5749 
<br/><br/><label>Standard No.: </label>10.1136/gut.2005.086769  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Aged<br/>Aged, 80 and over<br/>Case-Control Studies<br/>Celiac Disease--genetics<br/>Chi-Square Distribution<br/>Child<br/>Child, Preschool<br/>Female<br/>Gene Frequency<br/>Genetic Predisposition to Disease<br/>Haplotypes<br/>Humans<br/>Male<br/>Middle Aged<br/>Myosins--genetics<br/>Polymorphism, Single Nucleotide<br/>United Kingdom