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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

✍ Scribed by D. Noack; J. Rae; A.R. Cross; J. Muñoz; S. Salmen; J.A. Mendoza; N. Rossi; J.T. Curnutte; P.G. Heyworth

Publisher
Springer
Year
1999
Tongue
English
Weight
236 KB
Volume
105
Category
Article
ISSN
0340-6717

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Chronic granulomatous disease caused by
Chronic granulomatous disease caused by mutations other than the common GT deletion in NCF1, the gene encoding the p47phox component of the phagocyte NADPH oxidase
✍ Dirk Roos; Martin de Boer; M. Yavuz Köker; Jan Dekker; Vinita Singh-Gupta; Ander 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 688 KB

## For the Immunogenetics Special Issue Chronic granulomatous disease (CGD) is an inherited immunodeficiency caused by defects in any of four genes encoding components of the leukocyte nicotinamide dinucleotide phosphate, reduced (NADPH) oxidase. One of these is the autosomal neutrophil cytosolic