Associated Papers
Structure of the core human NADPH oxidase NOX2.
Noreng S et al.
Nature Communications, 2022
36241643 (PubMed )
Supplement: 41467_2022_33711_MOESM1_ESM.pdf
Chronic granulomatous disease associated with Duchenne muscular dystrophy caused by Xp21.1 contiguous gene deletion syndrome: Case report and literature review.
Bi S et al.
Frontiers in Genetics, 2022
Identification of a Novel Mutation in the CYBB Gene, p.Asp378Gly, in a Patient With X-linked Chronic Granulomatous Disease.
Song SM et al.
Allergy, Asthma & Immunology Research, 2014
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