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chronic granulomatous disease, autosomal, due to deficiency of cyba
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CYBA
RAGE and CYBA polymorphisms are associated with microalbuminuria and end-stage renal disease onset in a cohort of type 1 diabetes mellitus patients over a 20-year follow-up
Association of p22phox gene C242T polymorphism with coronary artery disease: a meta-analysis
Relationship of the p22phox (CYBA) gene polymorphism C242T with risk of coronary artery disease: a meta-analysis
The A640G polymorphism in the NAD(P)H oxidase p22phox gene (CYBA) is associated with risk reduction of coronary heart disease: a meta-analysis
Polymorphisms of C242T and A640G in CYBA gene and the risk of coronary artery disease: a meta-analysis
Meta-analysis of C242T polymorphism in CYBA genes: risk of acute coronary syndrome is lower in Asians but not in Caucasians
Human neutrophil cytochrome b light chain (p22-phox). Gene structure, chromosomal location, and mutations in cytochrome-negative autosomal recessive chronic granulomatous disease
Novel cytochrome b system in phagocytic vacuoles of human granulocytes
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