Associated Papers
Phenotypic spectrum in a family with a novel RAC2 p.I21S dominant-activating mutation.
Ashby L et al.
Clinical & Translational Immunology, 2024
Novel Loss of Function (G15D) Mutation on RAC2 in a Family with Combined Immunodeficiency and Increased Levels of Immunoglobulin G, A, and E.
Duan X et al.
Journal of Clinical Immunology, 2023
A Novel RAC2 Mutation Causing Combined Immunodeficiency.
Zhang L et al.
Journal of Clinical Immunology, 2023
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