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(Washington University in St. Louis), J T Curnutte, Stuart H. Orkin(Howard Hughes Medical Institute), Richard W. Erickson(Riley Hospital for Children), R Seger(Riley Hospital for Children), T. J. Mühlebach(Riley Hospital for Children), Hans A. Messner(University of Toronto), Eric A. Pierce(Broad Institute)
Proceedings of the National Academy of Sciences
December 15, 1991
Cited by 100


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