Skip to content Skip to footer

Research Portal of the TU Dresden

More severe than CVID: Combined immunodeficiency due to a novel NFKB2 mutation

Research output: Contribution to journal › Letter › Contributed › peer-review

Contributors

Marc Bienias - , TUD Dresden University of Technology (Author)
Anastasia Gabrielyan - , TUD Dresden University of Technology (Author)
Linda Geberzahn - , TUD Dresden University of Technology (Author)
Angela Rösen‐Wolff - , Department of Paediatrics (Author)
Angela Huebner - , Department of Paediatrics (Author)
Eva‐Maria Jacobsen - , Ulm University Medical Center (Author)
Nicole Toepfner - , Department of Paediatrics (Author)
Mingyan Fang - , BGI Group (Author)
Min Ae Lee‐Kirsch - , Department of Paediatrics (Author)
Joachim Roesler - , TUD Dresden University of Technology (Author)
Catharina Schuetz - , Department of Paediatrics (Author)

Details

Original language	English
Pages (from-to)	793-797
Number of pages	5
Journal	Pediatric Allergy and Immunology
Volume	32
Issue number	4
Publication status	Published - 28 Dec 2020
Peer-reviewed	Yes

External IDs

PubMed	33369776
Scopus	85099456499
ORCID	/0009-0003-6519-0482/work/143074876

Keywords

Keywords

Common Variable Immunodeficiency/diagnosis, Humans, Mutation, NF-kappa B p52 Subunit/genetics, Primary Immunodeficiency Diseases