Associated Papers
Re-evaluation of the contribution of TNFRSF13B variants to antibody deficiency.
Abolhassani H et al.
Journal of Human Immunity, 2025
TACI Mutations in Primary Antibody Deficiencies: A Nationwide Study in Greece.
Kakkas I et al.
Medicina (kaunas, Lithuania), 2021
The impact of rare and low-frequency genetic variants in common variable immunodeficiency (CVID).
Bisgin A et al.
Scientific Reports, 2021
33859323 (PubMed )
Supplement: 41598_2021_87898_MOESM2_ESM.pdf
Screening for primary immunodeficiency diseases by next-generation sequencing in early life.
Sun J et al.
Clinical & Translational Immunology, 2020
32431812 (PubMed )
Supplement: CTI2-9-e1138-s001.xlsx › Sheet1
Phenotypic and genotypic characterization of inflammatory bowel disease in children under six years of age in China.
Fang YH et al.
World Journal of Gastroenterology, 2018
Clinical Associations of Biallelic and Monoallelic TNFRSF13B Variants in Italian Primary Antibody Deficiency Syndromes.
Pulvirenti F et al.
Journal of Immunology Research, 2016
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