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chronic granulomatous disease, autosomal, due to deficiency of cyba
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CYBA
Primary structure and unique expression of the 22-kilodalton light chain of human neutrophil cytochrome b
Preliminary characterisation of the promoter of the human p22(phox) gene: identification of a new polymorphism associated with hypertension
Cytochrome b-558 alpha-subunit cloning and expression in rat aortic smooth muscle cells
Absence of both the 91kD and 22kD subunits of human neutrophil cytochrome b in two genetic forms of chronic granulomatous disease
Homologs of gp91phox: cloning and tissue expression of Nox3, Nox4, and Nox5
Direct interaction of the novel Nox proteins with p22phox is required for the formation of a functionally active NADPH oxidase
Functional analysis of Nox4 reveals unique characteristics compared to other NADPH oxidases
Critical roles for p22phox in the structural maturation and subcellular targeting of Nox3