Association of hereditary angioedema type 1 with developmental anomalies due to a large and unusual de novo pericentromeric rearrangement of chromosome 11 spanning the entire C1 inhibitor gene (SERPING1)

Publication date: Available online 16 October 2018

Source: The Journal of Allergy and Clinical Immunology: In Practice

Author(s): Ebo Didier G, Blaumeiser Bettina, Kooy R. Frank, Beckers Sigri, Van Gasse Athina L, Saerens Michael, Spinhoven Maarten, Sabato Vito, Poirel Hélène A