Hematologically important mutations: X-linked chronic granulomatous disease (third update)

Chronic granulomatous disease (CGD) is an immunodeficiency disorder affecting about 1 in 250,000 individuals. The disease is caused by a lack of superoxide production by the leukocyte enzyme NADPH oxidase. Superoxide is used to kill phagocytosed micro-organisms in neutrophils, eosinophils, monocytes...

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Veröffentlicht in:	Blood cells, molecules, & diseases molecules, & diseases, 2010-10, Vol.45 (3), p.246-265
Hauptverfasser:	Roos, Dirk, Kuhns, Douglas B., Maddalena, Anne, Roesler, Joachim, Lopez, Juan Alvaro, Ariga, Tadashi, Avcin, Tadej, de Boer, Martin, Bustamante, Jacinta, Condino-Neto, Antonio, Di Matteo, Gigliola, He, Jianxin, Hill, Harry R., Holland, Steven M., Kannengiesser, Caroline, Köker, M. Yavuz, Kondratenko, Irina, van Leeuwen, Karin, Malech, Harry L., Marodi, László, Nunoi, Hiroyuki, Stasia, Marie-José, Ventura, Anna Maria, Witwer, Carl T., Wolach, Baruch, Gallin, John I.
Format:	Artikel
Sprache:	eng
Schlagworte:	Chromosomes, Human, X Chromosomes, Human, X - genetics Chromosomes, Human, X - metabolism Chronic granulomatous disease CYBB gp91 phox Granulomatous Disease, Chronic Granulomatous Disease, Chronic - enzymology Granulomatous Disease, Chronic - epidemiology Granulomatous Disease, Chronic - genetics Humans Immunology Innate immunity Life Sciences Membrane Glycoproteins Membrane Glycoproteins - genetics Membrane Glycoproteins - metabolism Mutation NADPH Oxidase NADPH Oxidase 2 NADPH Oxidases - genetics NADPH Oxidases - metabolism Superoxides Superoxides - metabolism X-linked disease
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