Bonizzato, A <br/><br/>
Identification of a double mutation (D160V-K161E) in the p67phox gene of a chronic granulomatous disease patient.  [electronic resource] 

 -  Biochemical and biophysical research communications  Feb 1997 
 - 861-3 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0006-291X 
<br/><br/><label>Standard No.: </label>10.1006/bbrc.1997.6204  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Genes<br/>Granulomatous Disease, Chronic--genetics<br/>Humans<br/>Neutrophils--physiology<br/>Phosphoproteins--genetics<br/>Point Mutation<br/>Polymerase Chain Reaction<br/>Polymorphism, Single-Stranded Conformational