Novel duplication in the F12 gene in a patient with recurrent angioedema
Author:
Publisher
Elsevier BV
Subject
Immunology,Immunology and Allergy
Reference19 articles.
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2. International consensus on hereditary and acquired angioedema;Lang;Ann. Allergy Asthma Immunol.,2012
3. Genetically determined heterogeneity of the C1 esterase inhibitor in patients with hereditary angioneurotic edema;Rosen;J. Clin. Invest.,1971
4. Altered C1 inhibitor genes in type I hereditary angioedema;Stoppa-Lyonnet;N. Engl. J. Med.,1987
5. Missense mutations in the coagulation factor XII (Hageman factor) gene in hereditary angioedema with normal C1 inhibitor;Dewald;Biochem. Biophys. Res. Commun.,2006
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1. Hereditary angioedema with normal C1-inhibitor;Annals of Allergy, Asthma & Immunology;2024-06
2. In Silico Analysis and In-depth Assessment of a Female Patient with a Missense Mutation in the F12 Gene Associated with Hereditary Angioedema Symptoms: A Case Study;2023-10-04
3. Gene Mutations Linked to Hereditary Angioedema in Solitary Angioedema Patients With Normal C1 Inhibitor;The Journal of Allergy and Clinical Immunology: In Practice;2023-08
4. Genetic Variants Leading to Urticaria and Angioedema and Associated Biomarkers;The Journal of Allergy and Clinical Immunology: In Practice;2023-08
5. Angioedema With Normal Complement Studies: What Do We Know?;The Journal of Allergy and Clinical Immunology: In Practice;2023-08
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