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Heterozygous mutations in the C-terminal domain of COPA underlie a complex autoinflammatory syndrome
Download from doi.orgHuman Autosomal Recessive DNA Polymerase Delta 3 Deficiency Presenting as Omenn Syndrome
UploadHuman germline heterozygous gain-of-functionSTAT6variants cause severe allergic disease
UploadHuman type I IFN deficiency does not impair B cell response to SARS-CoV-2 mRNA vaccination
UploadHuman OTULIN haploinsufficiency impairs cell-intrinsic immunity to staphylococcal α-toxin
UploadHematopoietic Cell Transplantation Cures Adenosine Deaminase 2 Deficiency: Report on 30 Patients
UploadRecent advances in primary immunodeficiency: from molecular diagnosis to treatment
Download from doi.orgActivated PI3Kδ breaches multiple B cell tolerance checkpoints and causes autoantibody production
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