Associated Papers
Re-evaluation of the contribution of TNFRSF13B variants to antibody deficiency.
Abolhassani H et al.
Journal of Human Immunity, 2025
Genetic characteristics of common variable immunodeficiency patients with autoimmunity.
Liu Z et al.
Frontiers in Genetics, 2023
Germline variants in UNC13D and AP3B1 are enriched in COVID-19 patients experiencing severe cytokine storms.
Luo H et al.
European Journal of Human Genetics : Ejhg, 2021
33867526 (PubMed )
Supplement: 41431_2021_886_MOESM2_ESM.xlsx › TableS4
Screening for Genetic Mutations for the Early Diagnosis of Common Variable Immunodeficiency in Children With Refractory Immune Thrombocytopenia: A Retrospective Data Analysis From a Tertiary Children's Center.
Ma J et al.
Frontiers in Pediatrics, 2020
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