Chronic granulomatous disease caused by mutations other than the common GT deletion in NCF1, the gen...
Chronic granulomatous disease caused by mutations other than the common GT deletion in NCF1, the gene encoding the p47phox component of the phagocyte NADPH oxidase
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Publisher
Hoboken: Wiley Subscription Services, Inc., A Wiley Company
Journal title
Language
English
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Publication information
Publisher
Hoboken: Wiley Subscription Services, Inc., A Wiley Company
Subjects
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Scope and Contents
Contents
Chronic granulomatous disease (CGD) is an inherited immunodeficiency caused by defects in any of four genes encoding components of the leukocyte nicotinamide dinucleotide phosphate, reduced (NADPH) oxidase. One of these is the autosomal neutrophil cytosolic factor 1 (NCF1) gene encoding the p47phoxprotein. Most (>97%) CGD patients without p47phox (...
Alternative Titles
Full title
Chronic granulomatous disease caused by mutations other than the common GT deletion in NCF1, the gene encoding the p47phox component of the phagocyte NADPH oxidase
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Record Identifier
TN_cdi_proquest_miscellaneous_68979935
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_68979935
Other Identifiers
ISSN
1059-7794
E-ISSN
1098-1004
DOI
10.1002/humu.20413
