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, Anders Åhlin, Jan Palmblad, Özden Sanal, Magdalena Kurenko-Deptuch, Stephen Jolles, Baruch Wolach

*Corresponding author for this work

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Biochemistry, Genetics and Molecular Biology