More severe than CVID: Combined immunodeficiency due to a novel NFKB2 mutation.
Pediatr Allergy Immunol
; 32(4): 793-797, 2021 05.
Article
in En
| MEDLINE
| ID: mdl-33369776
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Common Variable Immunodeficiency
/
Primary Immunodeficiency Diseases
Type of study:
Diagnostic_studies
Limits:
Humans
Language:
En
Journal:
Pediatr Allergy Immunol
Journal subject:
ALERGIA E IMUNOLOGIA
/
PEDIATRIA
Year:
2021
Document type:
Article
Affiliation country:
Alemania
Country of publication:
Reino Unido