Severe congenital neutropenia due to jagunal homolog 1 (JAGN1) mutation: a case report and literature review.
Front Pediatr
; 11: 1223191, 2023.
Article
in En
| MEDLINE
| ID: mdl-37528877
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Language:
En
Journal:
Front Pediatr
Year:
2023
Document type:
Article
Affiliation country:
United States
Country of publication:
Switzerland