Clinical, immunological and genetic findings in patients with UNC13D deficiency (FHL3): A systematic review.
Pediatr Allergy Immunol
; 32(1): 186-197, 2021 01.
Article
in En
| MEDLINE
| ID: mdl-32679608
Key words
Full text:
1
Database:
MEDLINE
Main subject:
Lymphohistiocytosis, Hemophagocytic
/
Immunologic Deficiency Syndromes
Type of study:
Diagnostic_studies
/
Screening_studies
/
Systematic_reviews
Limits:
Humans
Language:
En
Year:
2021
Type:
Article