Publication
Title
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)
Author
Ebo, Didier G.
Blaumeiser, Bettina
Kooy, R. Frank
Beckers, Sigri
Van Gasse, Athina L.
Saerens, Michael
Spinhoven, Maarten
Sabato, Vito
Poirel, Hélène A.
Language
English
Source (journal)
The journal of allergy and clinical immunology. In practice. - New York, NY, 2013, currens
The journal of allergy and clinical immunology. In practice. - New York, NY, 2013, currens
Publication
Amsterdam
:
Elsevier science bv
,
2019
ISSN
2213-2198
Volume/pages
7 :4 (2019) , p. 1352-+
ISI
000463732500045
Pubmed ID
30336291
Full text (Publisher's DOI)
https://doi.org/10.1016/J.JAIP.2018.10.005
Full text (open access)
https://repository.uantwerpen.be/docman/irua/30a356/155006_2019_10_17.pdf
UAntwerpen
Faculty/Department
Faculty of Medicine and Health Sciences
Faculty of Pharmaceutical, Biomedical and Veterinary Sciences . Biomedical Sciences
Research group
Translational Pathophysiological Research (TPR)
Medical Genetics (MEDGEN)
Cognitive Genetics (COGNET)
Project info
GENOMED - Genomics in Medicine.
Publication type
L1 Letter to the editor
Subject
Biology
Human medicine
Affiliation
Publications with a UAntwerp address
External links
Web of Science
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Record
Identification
Creation
19.11.2018
Last edited
23.09.2021
To cite this reference
https://hdl.handle.net/10067/1550060151162165141