Keywords = p47Phox
An Iranian Patient Suffering from Chronic Granulomatous Disease, with Mutation in the NCF1 Gene

Volume 3, Issue 1, March 2020, Pages 64-70

10.22034/igj.2020.225558.1037

Fereshte Salami; Ronak Mozafari Nezhad; Sahar Shariati; Babak Mirminachi