A Novel Heterozygous NFKB2 Variant in a Multiplex Family with Common Variable Immune Deficiency and Autoantibodies Against Type I IFNs

Common Variable Immunodeficiency Primary Immunodeficiency Hypogammaglobulinemia Immune Dysregulation
DOI: 10.1007/s10875-024-01843-1 Publication Date: 2024-11-23T07:35:25Z