Human neutrophil cytochrome b light chain (p22-phox). Gene structure, chromosomal location, and mutations in cytochrome-negative autosomal recessive chronic granulomatous disease.Mary C. Dinauer, Stuart H. Orkin, Eric A. Pierce et al.|Journal of Clinical Investigation|1990Cited by 329
Point mutation in the cytoplasmic domain of the neutrophil p22-phox cytochrome b subunit is associated with a nonfunctional NADPH oxidase and chronic granulomatous disease.Mary C. Dinauer, J T Curnutte, Eric A. Pierce et al.|Proceedings of the National Academy of Sciences|1991Cited by 100