Identification of allele-specific p22-ph
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Johann Peter Hossle; Martin Boer; Reinhard A. Seger; Dirk Roos
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Article
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1994
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Springer
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English
โ 968 KB
A rare subgroup (approx. 5%) of all chronic granulomatous disease (CGD) patients suffers from mutations in the gene encoding the small p22-phox subunit of the flavocytochrome b558 heterodimer, the terminal redox component of the phagocyte NADPH oxidase. A male CGD patient with neutrophil granulocyte