Last Updated: 09/26/2026
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Found 4 publications
Combined immunodeficiency with autoimmunity caused by a homozygous missense mutation in inhibitor of nuclear factor 𝛋B kinase alpha (IKKα).
Journal: Science immunology
Published: September 17, 2021
A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency.
Journal: The Journal of allergy and clinical immunology
Published: October 24, 2018
T-cell mitochondrial dysfunction and lymphopenia in DOCK2-deficient patients.
Journal: The Journal of allergy and clinical immunology
Published: October 22, 2018
A digenic human immunodeficiency characterized by IFNAR1 and IFNGR2 mutations.
Journal: The Journal of clinical investigation
Published: February 17, 2017
Showing 1-4 of 4
Last Updated: 09/26/2026