Takada, H <br/><br/>
NEMO mutation as a cause of familial occurrence of Behçet's disease in female patients.  [electronic resource] 

 -  Clinical genetics  Dec 2010 
 - 575-9 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1399-0004 
<br/><br/><label>Standard No.: </label>10.1111/j.1399-0004.2010.01432.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Base Sequence<br/>Behcet Syndrome--genetics<br/>Child<br/>Female<br/>Heterozygote<br/>Humans<br/>I-kappa B Kinase--genetics<br/>Molecular Sequence Data<br/>Mutation<br/>X Chromosome Inactivation--genetics