Common variable immunodeficiency in two kindreds with heterogeneous phenotypes caused by novel heterozygous NFKB1 mutations
Frederik Staels(KU Leuven), Rik Schrijvers(Vestigia)
Cited by 6
Related Papers
A Novel Homozygous Stop Mutation in IL23R Causes Mendelian Susceptibility to Mycobacterial Disease
|Journal of Clinical Immunology|2022|21