Less severe clinical manifestations in patients with hereditary angioedema with missense C1INH gene mutations
Author:
Publisher
Elsevier BV
Subject
Immunology,Immunology and Allergy
Reference16 articles.
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3. Angioedema due to C1 inhibitor deficiency in 2010;Cicardi;Intern Emerg Med,2010
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1. The CC2D2B is a novel genetic modifier of the clinical phenotype in patients with hereditary angioedema due to C1 inhibitor deficiency;Gene;2024-08
2. Application of a dried blood spot based proteomic and genetic assay for diagnosing hereditary angioedema;Clinical and Translational Allergy;2023-11
3. Myeloid lineage cells evince distinct steady-state level of certain gene groups in dependence on hereditary angioedema severity;Frontiers in Genetics;2023-07-04
4. Searching for Genetic Biomarkers for Hereditary Angioedema Due to C1-Inhibitor Deficiency (C1-INH-HAE);Frontiers in Allergy;2022-07-07
5. SERPING1 Variants and C1-INH Biological Function: A Close Relationship With C1-INH-HAE;Frontiers in Allergy;2022-03-31
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