Clinical and molecular findings of chronic granulomatous disease in Oman: family studies
Author:
Affiliation:
1. Department of Child Health; Sultan Qaboos University Hospital; Muscat Oman
2. INSERM, UMR_S 665; INSERM; Paris France
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference12 articles.
1. Chronic granulomatous disease; fundamental stages in our understanding of CGD;Assari;Med Immunol,2006
2. Hematologically important mutations: X-linked chronic granulomatous disease (third update);Roos;Blood Cells Mol Dis,2010
3. A new genetic subgroup of chronic granulomatous disease with autosomal recessive mutations in p40phox and selective defects in neutrophil NADPH oxidase activity;Matute;Blood,2009
4. Autosomal recessive chronic granulomatous disease caused by defects in NCF1, the gene encoding the phagocyte p47phox: mutations not arising in the NCF1 pseudogenes;Noack;Blood,2001
5. Hematologically important mutations: the autosomal recessive forms of chronic granulomatous disease (second update);Roos;Blood Cells Mol Dis,2010
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1. Chronic granulomatous disease in the United Arab Emirates: clinical and molecular characteristics in a single center;Frontiers in Immunology;2023-11-02
2. The Risk of the Next Child Getting Affected by Chronic Granulomatous Disease in Families with at Least One Autosomal Recessive CGD Child;Iranian Journal of Allergy, Asthma and Immunology;2023-02-25
3. Chronic granulomatous disease associated with Duchenne muscular dystrophy caused by Xp21.1 contiguous gene deletion syndrome: Case report and literature review;Frontiers in Genetics;2023-01-13
4. Genetic Causes, Clinical Features, and Survival of Underlying Inborn Errors of Immunity in Omani Patients: a Single-Center Study;Journal of Clinical Immunology;2022-11-03
5. Hematologically important mutations: The autosomal forms of chronic granulomatous disease (third update);Blood Cells, Molecules, and Diseases;2021-12
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