Pearce, S H <br/><br/>
A common and recurrent 13-bp deletion in the autoimmune regulator gene in British kindreds with autoimmune polyendocrinopathy type 1.  [electronic resource] 

 -  American journal of human genetics  Dec 1998 
 - 1675-84 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0002-9297 
<br/><br/><label>Standard No.: </label>10.1086/302145  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Base Sequence<br/>Chromosomes, Human, Pair 21--genetics<br/>Exons--genetics<br/>Female<br/>Founder Effect<br/>Genotype<br/>Haplotypes--genetics<br/>Humans<br/>Male<br/>Molecular Sequence Data<br/>Nuclear Family<br/>Pedigree<br/>Point Mutation--genetics<br/>Polyendocrinopathies, Autoimmune--genetics<br/>Polymorphism, Single-Stranded Conformational<br/>Sequence Analysis, DNA<br/>Sequence Deletion<br/>Transcription Factors--genetics<br/>United Kingdom<br/>AIRE Protein