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)
Titel:
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)
Auteur:
Ebo, Didier G. Blaumeiser, Bettina Kooy, Frank R. Beckers, Sigri Van Gasse, Athina L. Saerens, Michael Spinhoven, Maarten Sabato, Vito Poirel, Hélène A.
Verschenen in:
The journal of allergy and clinical immunology. In practice