Expanding the Clinical Phenotype of Autosomal Recessive Chronic Granulomatous Disease
Author:
Funder
National Cancer Institute, National Institutes of Health
Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s10875-024-01782-x.pdf
Reference5 articles.
1. Yu HH, Yang YH, Chiang BL. Chronic granulomatous disease: a Comprehensive Review. Clin Rev Allergy Immunol 2020 612. 2020;61(2):101–13. https://doi.org/10.1007/S12016-020-08800-X.
2. Kuhns DB, Alvord WG, Heller T, et al. Residual NADPH oxidase and survival in chronic Granulomatous Disease. N Engl J Med. 2010;363(27):2600–10.
3. Van De Geer A, Nieto-Patlán A, Kuhns DB, et al. Inherited p40phox deficiency differs from classic chronic granulomatous disease. J Clin Invest. 2018;128(9):3957.
4. Matute JD, Arias AA, Wright NA, Wrobel I, Waterhouse CC, Li XJ, Marchal CC, Stull ND, Lewis DB, Steele M, Kellner JD, Yu W, Meroueh SO, Nauseef WM, Dinauer MC. A new genetic subgroup of chronic granulomatous disease with autosomal recessive mutations in p40 phox and selective defects in neutrophil NADPH oxidase activity. Blood. 2009;114(15):3309–15.
5. Wright M, Chandrakasan S, Okou DT, Yin H, Jurickova I, Denson LA, Kugathasan S. Early Onset Granulomatous Colitis Associated with a mutation in NCF4 resolved with hematopoietic stem cell transplantation. J Pediatr. 2019;210:220–5.
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