Associated Papers
Expanding clinical phenotype of truncating activation-induced cytidine deaminase variants.
Kuipers C et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology, 2025
A Novel Heterozygous Variant in AICDA Impairs Ig Class Switching and Somatic Hypermutation in Human B Cells and is Associated with Autosomal Dominant HIGM2 Syndrome.
Della Mina E et al.
Journal of Clinical Immunology, 2024
A novel activation-induced cytidine deaminase (AID) mutation in Brazilian patients with hyper-IgM type 2 syndrome.
Caratão N et al.
Clinical Immunology (orlando, Fla.), 2013
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