de Boer, M <br/><br/>
Autosomal recessive chronic granulomatous disease with absence of the 67-kD cytosolic NADPH oxidase component: identification of mutation and detection of carriers.  [electronic resource] 

 -  Blood  Jan 1994 
 - 531-6 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0006-4971 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Base Sequence<br/>Child<br/>Female<br/>Granulomatous Disease, Chronic--enzymology<br/>Heterozygote<br/>Humans<br/>Molecular Sequence Data<br/>Mutation<br/>NADH, NADPH Oxidoreductases--deficiency<br/>NADPH Oxidases