Hereditary Angioedema Due to C1 Inhibitor Deficiency in Serbia: Two Novel Mutations and Evidence of Genotype-Phenotype Association
Author:
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
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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. Normalization of C1 Inhibitor in a Patient with Hereditary Angioedema;New England Journal of Medicine;2024-07-04
3. Systematic Approach Revealed SERPING1 Splicing-Affecting Variants to be Highly Represented in the Czech National HAE Cohort;Journal of Clinical Immunology;2023-08-25
4. National survey on clinical and genetic characteristics of patients with hereditary angioedema in Latvia;Allergy, Asthma & Clinical Immunology;2023-04-08
5. Hereditary Angioedema: Diagnosis, Clinical Implications, and Pathophysiology;Advances in Therapy;2023-01-07
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