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Protein functionality as a potential bottleneck for somatic revertant variants
Loss of ZBTB24 impairs nonhomologous end-joining and class-switch recombination in patients with ICF syndrome
Delineating Human B Cell Precursor Development With Genetically Identified PID Cases as a Model
Repertoire Sequencing of B Cells Elucidates the Role of UNG and Mismatch Repair Proteins in Somatic Hypermutation in Humans
IVIg-induced plasmablasts in patients with Guillain-Barre syndrome
No Overt Clinical Immunodeficiency Despite Immune Biological Abnormalities in Patients With Constitutional Mismatch Repair Deficiency
Adaptive antibody diversification through N-linked glycosylation of the immunoglobulin variable region
Identification of checkpoints in human T-cell development using severe combined immunodeficiency stem cells
Similar recombination-activating gene (RAG) mutations result in similar immunobiological effects but in different clinical phenotypes
SIMILAR N-TERMINAL TRUNCATING RAG1 MUTATIONS GIVE RISE TO A BROAD SPECTRUM OF CLINICAL PHENOTYPES
Artemis splice defects cause atypical SCID and can be restored in vitro by an antisense oligonucleotide