Nine novel HOGA1 gene mutations identified in primary hyperoxaluria type 3 and distinct clinical and biochemical characteristics in Chinese children.
Pediatr Nephrol
; 34(10): 1785-1790, 2019 10.
Article
in En
| MEDLINE
| ID: mdl-31123811
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Hyperoxaluria, Primary
/
Urolithiasis
/
Oxo-Acid-Lyases
Type of study:
Diagnostic_studies
/
Observational_studies
/
Prognostic_studies
/
Risk_factors_studies
Limits:
Child, preschool
/
Female
/
Humans
/
Infant
/
Male
Country/Region as subject:
Asia
Language:
En
Journal:
Pediatr Nephrol
Journal subject:
NEFROLOGIA
/
PEDIATRIA
Year:
2019
Type:
Article
Affiliation country:
China