| 1 | GDCC2, NCF2
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| A 1.1-kb duplication in the p67-phox gene causes chronic granulomatous disease.
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| Borgato L, Bonizzato A, Lunardi C, Dusi S, Andrioli G, Scarperi A, Corrocher R.
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| Hum Genet 108(6):504-10. 2001
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| 2 | GDCC2, NCF2
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| Autosomal recessive chronic granulomatous disease caused by novel mutations in NCF-2, the gene encoding the p67-phox component of phagocyte NADPH oxidase.
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| Noack D, Rae J, Cross AR, Munoz J, Salmen S, Mendoza JA, Rossi N, Curnutte JT, Heyworth PG.
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| Hum Genet 105(5):460-7 1999
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| 3 | GDCC2, NCF2
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| Identification of a double mutation (D160V-K161E) in the p67phox gene of a chronic granulomatous disease patient.
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| Bonizzato A, et al.
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| Biochem Biophys Res Commun 231 : 861-863. 1997
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| 4 | GDCC2, NCF2
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| Two-exon skipping due to a point mutation in p67-phox-deficient chronic granulomatous disease.
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| Aoshima M, et al.
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| Blood 88 : 1841-1845. 1996
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| 5 | GDCC2, NCF2
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| A mutation located at the 5' splice junction sequence of intron 3 in the p67phox gene causes the lack of p67phox mRNA in a patient with chronic granulomatous disease.
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| Cohen Tanugi-Cholley L, et al.
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| Blood 85 : 242-249. 1995
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| 6 | GDCC2, NCF2
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| Autosomal recessive chronic granulomatous disease with absence of the 67-kD cytosolic NADPH oxidase component : identification of mutation and detection of carriers.
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| De Boer M, et al.
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| Blood 83 : 531-536. 1994
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| 7 | GDCC2, NCF1, NCF2
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| Genes for two autosomal recessive forms of chronic granulomatous disease assigned to 1q25 (NCF2) and 7q11.23 (NCF1).
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| Francke U, et al.
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| Am J Hum Genet 47 : 483-492. 1990
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| 8 | CYBA, CYBB, GDCC2, NCF1, NCF2
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| Genetic variants of chronic granulomatous disease : prevalence of deficiencies of two cytosolic components of the NADPH oxidase system.
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| Clark RA, et al.
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| N Engl J Med 321 : 647-652. 1989
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