
Mutation in IRF2BP2 is responsible for a familial form of common variable immunodeficiency disorder
Keywords: Common variable immunodeficiency; machine learning; primary antibody deficiency; IRF2BP2; immunoglobulin; CNV; Copy number variation; CVID; Common variable immunodeficiency disorder; EBV-LCL; EBV-immortalized lymphoblastoid cell line; SNP; Single nucleoti