Rubin, Tamar S <br/><br/>
Newborn Screening for IKBKB Deficiency in Manitoba, Using Genetic Mutation Analysis.  [electronic resource] 

 -  Journal of clinical immunology  10 2018 
 - 742-744 p.  digital 
<br/><br/> Publication Type: Letter 
<br/><br/><label>ISSN: </label>1573-2592 
<br/><br/><label>Standard No.: </label>10.1007/s10875-018-0555-2  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>DNA Mutational Analysis<br/>Genetic Association Studies<br/>Genetic Predisposition to Disease<br/>Genotype<br/>Humans<br/>I-kappa B Kinase--deficiency<br/>Infant, Newborn<br/>Mutation<br/>Neonatal Screening<br/>Phenotype<br/>Severe Combined Immunodeficiency--diagnosis