Associated Papers
A novel homozygous frameshift mutation likely causing nonsense-mediated mRNA decay in an Algerian kindred with CD19 complex deficiency.
Belaid B et al.
Frontiers in Immunology, 2025
Evaluating the Genetics of Common Variable Immunodeficiency: Monogenetic Model and Beyond.
de Valles-Ibáñez G et al.
Frontiers in Immunology, 2018
29867916 (PubMed )
Supplement: data_sheet_1.PDF
Human CD19 and CD40L deficiencies impair antibody selection and differentially affect somatic hypermutation.
van Zelm MC et al.
The Journal of Allergy and Clinical Immunology, 2014
Antibody deficiency due to a missense mutation in CD19 demonstrates the importance of the conserved tryptophan 41 in immunoglobulin superfamily domain formation.
van Zelm MC et al.
Human Molecular Genetics, 2011
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