Mutations in the promoter region of the gene for gp91-phox in X-linked chronic granulomatous disease with decreased expression of cytochrome b558.

We examined the molecular defect in two kindreds with "variant" X-linked chronic granulomatous disease (CGD). Western blots of neutrophil extracts showed decreased immunoreactive cytochrome b558 components gp91-phox and p22-phox. Analysis of mRNA demonstrated reduced gp91-phox transcripts, with rela...

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Detaylı Bibliyografya
Yayımlandı:	J Clin Invest
Asıl Yazarlar:	Newburger, P E, Skalnik, D G, Hopkins, P J, Eklund, E A, Curnutte, J T
Materyal Türü:	Artigo
Dil:	Inglês
Baskı/Yayın Bilgisi:	American Society for Clinical Investigation 1994
Konular:	Research Article
Online Erişim:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC295199/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8083361/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI117437
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Mutations in the promoter region of the gene for gp91-phox in X-linked chronic granulomatous disease with decreased expression of cytochrome b558.

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