Dinauer, M. C., Pierce, E. A., Erickson, R. W., Muhlebach, T. J., Messner, H., Orkin, S. H., . . . Curnutte, J. T. (1991). 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. Proc Natl Acad Sci U S A.
Citación estilo ChicagoDinauer, M C., E A. Pierce, R W. Erickson, T J. Muhlebach, H. Messner, S H. Orkin, R A. Seger, and J T. Curnutte. "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." Proc Natl Acad Sci U S A 1991.
Cita MLADinauer, M C., et al. "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." Proc Natl Acad Sci U S A 1991.