Skip to Main Content

Paper Details

Specific antibody deficiency and autoinflammatory disease extend the clinical and immunological spectrum of heterozygous NFKB1 loss-of-function mutations in humans.
Haematologica
29
2016
NFKB1, antibody deficiency, autoinflammatory disease, humans
Author NameAffiliation
Michael GombertHematology and Clinical Immunology, University Children's Hospital, Heinrich-Heine-University
Arndt BorkhardtHematology and Clinical Immunology, University Children's Hospital, Heinrich-Heine-University
Arndt BorkhardtHematology and Clinical Immunology, University Children's Hospital, Heinrich-Heine-University
Ute FischerHematology and Clinical Immunology, University Children's Hospital, Heinrich-Heine-University
  • 1 - 4

Datasets

Release 1.2