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Correction to: Genes & Immunity https://doi.org/10.1038/s41435-024-00255-w, published online 24 January 2024 In this article the affiliation details for A. Cobat and B. Boisson were incorrectly given as: A. Cobat4, B. Boisson4,5, but should have been: A. Cobat4,5,13, B.
Abstract Primary antiphospholipid syndrome is characterized by thrombosis and autoantibodies directed against phospholipids or associated proteins. The genetic etiology of PAPS remains unknown. We enrolled 21 patients with thromboembolic events associated to lupus anticoagulant, anticardiolipin and anti β2 glycoprotein1 autoantibodies. We performed whole exome sequencing. Data were compared to public databases and to a control cohort of 873 non-autoimmune patients.
To view the full text, please login as a subscribed user or purchase a subscription. Click here to view the full text on ScienceDirect. The majority of patients with early-onset infections and agammaglobulinemia have recessive mutations that impair downstream signaling through the B cell- and pre-B cell-receptors.
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