Wong, Serre-Yu <br/><br/>
A RAG1 mutation found in Omenn syndrome causes coding flank hypersensitivity: a novel mechanism for antigen receptor repertoire restriction.  [electronic resource] 

 -  Journal of immunology (Baltimore, Md. : 1950)  Sep 2008 
 - 4124-30 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1550-6606 
<br/><br/><label>Standard No.: </label>10.4049/jimmunol.181.6.4124  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Motifs--genetics<br/>Amino Acid Substitution--genetics<br/>Animals<br/>Arginine--genetics<br/>CHO Cells<br/>Catalytic Domain--genetics<br/>Cricetinae<br/>Cricetulus<br/>Gene Rearrangement, beta-Chain T-Cell Antigen Receptor<br/>Genes, T-Cell Receptor beta--genetics<br/>Glutamine--genetics<br/>Homeodomain Proteins--genetics<br/>Humans<br/>Mice<br/>Mutagenesis, Site-Directed<br/>Severe Combined Immunodeficiency--enzymology<br/>VDJ Recombinases--genetics