Talebi, Taravat <br/><br/>
A Novel Non-frameshift ADA Deletion Detected by Whole Exome Sequencing in an Iranian Family with Severe Combined Immunodeficiency.  [electronic resource] 

 -  Iranian journal of allergy, asthma, and immunology  Feb 2020 
 - 94-101 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1735-5249 
<br/><br/><label>Standard No.: </label>10.18502/ijaai.v19i1.2422  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adenosine Deaminase--deficiency<br/>Agammaglobulinemia--genetics<br/>Female<br/>Humans<br/>Infant<br/>Iran<br/>Male<br/>Mutation<br/>Pedigree<br/>Severe Combined Immunodeficiency--genetics<br/>Exome Sequencing