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Identification of a novel NCF-1 (p47- phox ) pseudogene not containing the signature GT deletion: significance for A47° chronic granulomatous disease carrier detection
Blood (2002) 100 (5): 1845–1851.
Autosomal recessive chronic granulomatous disease caused by defects in NCF-1 , the gene encoding the phagocyte p47- phox : mutations not arising in the NCF-1 pseudogenes
Deborah Noack, Julie Rae, Andrew R. Cross, Beverly A. Ellis, Peter E. Newburger, John T. Curnutte, Paul G. Heyworth
Blood (2001) 97 (1): 305–311.
Molecular analysis of 9 new families with chronic granulomatous disease caused by mutations in CYBA , the gene encoding p22 phox
Blood (2000) 96 (3): 1106–1112.
Functional Analysis of NADPH Oxidase in Granulocytic Cells Expressing a ▵488-497 gp91 phox Deletion Mutant
Blood (1999) 94 (7): 2497–2504.