Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans

Overview of attention for article published in The Journal of Allergy and Clinical Immunology, March 2018

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Sociedad Ecuatoriana De Alergia,asma E Inmunologia (SEAAI), 25 Oct 2018

Results Both sporadic and familial cases demonstrated evidence of the noninfective complications of CVID, including massive…

Journal of Allergy and Clinical Immunology, 25 Oct 2018

The genetic cause of primary immunodeficiency disease holds prognostic implications. Tuijnenburg et al. have used whole-genome…

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