UGT1A1*6 mutation associated with the occurrence and severity in infants with prolonged jaundice.
Front Pediatr
; 10: 1080212, 2022.
Article
in En
| MEDLINE
| ID: mdl-36605758
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Type of study:
Observational_studies
/
Prognostic_studies
/
Risk_factors_studies
Language:
En
Journal:
Front Pediatr
Year:
2022
Document type:
Article
Affiliation country:
China
Country of publication:
Switzerland