Jahic, Amir <br/><br/>
A polymorphic Alu insertion that mediates distinct disease-associated deletions.  [electronic resource] 

 -  European journal of human genetics : EJHG  08 2016 
 - 1371-4 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1476-5438 
<br/><br/><label>Standard No.: </label>10.1038/ejhg.2016.20  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adenosine Triphosphatases--genetics<br/>Alleles<br/>Alu Elements--genetics<br/>Chromosome Breakpoints<br/>Exons<br/>Gene Deletion<br/>Homologous Recombination<br/>Humans<br/>Mutagenesis, Insertional<br/>Paraplegia--diagnosis<br/>Polymorphism, Genetic<br/>Spastic Paraplegia, Hereditary--diagnosis<br/>Spastin