D. Schubert

Phenotype, penetrance, and treatment of 133 cytotoxic T‐lymphocyte antigen 4–insufficient subjects

O. Elemento, T. Giese, A. Schulz, 2018, The Journal of allergy and clinical immunology.

Activating PI3Kδ mutations in a cohort of 669 patients with primary immunodeficiency

B. Fevang, A. Schmitt-Graeff, Z. Eskandarian, 2016, Clinical and experimental immunology.

Assessing the Functional Relevance of Variants in the IKAROS Family Zinc Finger Protein 1 (IKZF1) in a Cohort of Patients With Primary Immunodeficiency

C. Smulski, Z. Eskandarian, A. Bulashevska, 2019, Front. Immunol..

Autosomal-dominant immune dysregulation syndrome in humans with CTLA4 mutations

A. Schäffer, R. Backofen, S. Ehl, 2014, Nature Medicine.

Plasma cell deficiency in human subjects with heterozygous mutations in Sec61 translocon alpha 1 subunit (SEC61A1)

A. Schäffer, H. Cao, J. Puck, 2017, The Journal of allergy and clinical immunology.

Plasma cell deficiency in humans with heterozygous mutations in SEC61A1

A. Schäffer, H. Cao, J. Puck, 2017 .

Autosomal-dominant immune dysregulation syndrome in humans with CTLA4 mutations

A. Schäffer, R. Backofen, S. Ehl, 2014, Nature Medicine.