Associated Papers
Characterization of 4 New Mutations in the CYBB Gene in 10 Iranian Families With X-linked Chronic Granulomatous Disease.
Teimourian S et al.
Journal of Pediatric Hematology/oncology, 2018
Genetical analysis of all Danish patients diagnosed with chronic granulomatous disease.
Jakobsen MA et al.
Scandinavian Journal of Immunology, 2012
Hematologically important mutations: the autosomal recessive forms of chronic granulomatous disease (second update).
Roos D et al.
Blood Cells, Molecules & Diseases, 2010
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.
Roos D et al.
Human Mutation, 2006
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