Badalzadeh, Mohsen <br/><br/>
Molecular analysis of four cases of chronic granulomatous disease caused by defects in NCF-2: the gene encoding the p67-phox.  [electronic resource] 

 -  Iranian journal of allergy, asthma, and immunology  Dec 2012 
 - 340-4 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1735-1502 
<br/><br/><label>Standard No.: </label>011.04/ijaai.340344  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child<br/>Child, Preschool<br/>Codon, Nonsense<br/>DNA Mutational Analysis<br/>Exons<br/>Female<br/>Genetic Predisposition to Disease<br/>Granulomatous Disease, Chronic--enzymology<br/>Homozygote<br/>Humans<br/>Male<br/>Mutation<br/>NADPH Oxidases--deficiency<br/>Phenotype<br/>Phosphoproteins--deficiency<br/>Sequence Deletion