Publication | Open Access

A Hypermorphic Missense Mutation in PLCG2 , Encoding Phospholipase Cγ2, Causes a Dominantly Inherited Autoinflammatory Disease with Immunodeficiency

Encoding Phospholipase Cγ2Signal TransductionDisease MechanismAutoinflammatory DisordersPathogenesisImmunologyImmunodeficienciesPathologyHypermorphic Missense MutationImmunologic DiseaseAutoinflammatory DiseaseMedicineInborn Error Of Immunity