Point mutation in the cytoplasmic domain of the neutrophil p22-phox cytochrome b subunit is associated with a nonfunctional NADPH oxidase and chronic granulomatous disease.

Chronic granulomatous disease (CGD) is a congenital disorder in which phagocytes cannot generate superoxide (O2-) and other microbial oxidants due to mutations in any one of four components of the O2(-)-generating complex, NADPH oxidase. We report here a female CGD patient in whom a missense mutatio...

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Bibliografische gegevens

Gepubliceerd in:	Proc Natl Acad Sci U S A
Hoofdauteurs:	Dinauer, M C, Pierce, E A, Erickson, R W, Muhlebach, T J, Messner, H, Orkin, S H, Seger, R A, Curnutte, J T
Formaat:	Artigo
Taal:	Inglês
Gepubliceerd in:	National Academy of Sciences 1991
Onderwerpen:	Research Article
Online toegang:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC53108/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1763037/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.88.24.11231
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