Publication | Open Access

Mutation in IRF2BP2 is responsible for a familial form of common variable immunodeficiency disorder

Primary ImmunodeficiencyGenetic DisorderGeneticsPathogenesisImmunodeficienciesImmunologyPathologyGenetic EpidemiologySyndromic ImmunodeficienciesInborn Error Of ImmunityDisease Gene IdentificationMedicineFamilial Form