Specific antibody deficiency and autoinflammatory disease extend the clinical and immunological spectrum of heterozygous NFKB1 loss-of-function mutations in humans
Document Type: | Article |
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Language: | English |
Author: | Cyrill Schipp, Schafiq Nabhani, Kirsten Bienemann, Natalia Simanovsky, Shlomit Kfir-Erenfeld, Nathalie Assayag-Asherie, Prasad T. Oommen, Shoshana Revel-Vilk, Andrea Hönscheid, Michael Gombert, Sebastian Ginzel, Daniel Schafer, Hans-Jurgen Laws, Eitan Yefenof, Bernhard Fleckenstein, Arndt Borkhardt, Polina Stepensky, Ute Fischer |
Parent Title (English): | Haematologica |
Volume: | 101 |
Issue: | 10 |
First Page: | 392 |
Last Page: | 396 |
ISSN: | 1592-8721 |
DOI: | https://doi.org/10.3324/haematol.2016.145136 |
PMID: | https://pubmed.ncbi.nlm.nih.gov/27365489 |
Publisher: | Ferrata Storti Foundation |
Date of first publication: | 2016/10/01 |
Keyword: | Fas; NFKB; antibody deficiency; autoimmune lymphoproliferative syndrome; autoinflammatory disease; immunodeficiency |
Departments, institutes and facilities: | Fachbereich Informatik |
Dewey Decimal Classification (DDC): | 6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit |
Entry in this database: | 2017/03/02 |