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Cytochrome b deficiency in an autosomal form of chronic granulomatous disease. A third form of chronic granulomatous disease recognized by monocyte hybridization.

Three patients (two sisters and a brother) in one family are described with chronic granulomatous disease. The granulocytes of these patients did not respond with a metabolic burst to various stimuli and failed to kill catalase-positive microorganisms. The magnitude of the cytochrome b signal in the...

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Detalhes bibliográficos
Publicado no:J Clin Invest
Main Authors: Weening, R S, Corbeel, L, de Boer, M, Lutter, R, van Zwieten, R, Hamers, M N, Roos, D
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Clinical Investigation 1985
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC423624/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/3980731/
https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI111792
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