bibliographic entry 12697161 [be/12697161]
https://w3id.org/oc/corpus/be/12697161
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Roos, D, de Boer, M, Koker, M.Y. 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, Hum. Mutat, 27, 2006, 1218, 1229, PMID: 16972229
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