Clinical and laboratory features of Macedonian children with OCRL mutations.
Pediatr Nephrol
; 26(4): 557-62, 2011 Apr.
Article
in En
| MEDLINE
| ID: mdl-21249396
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Phosphoric Monoester Hydrolases
/
Dent Disease
/
Oculocerebrorenal Syndrome
Limits:
Child
/
Humans
/
Infant
Country/Region as subject:
Europa
Language:
En
Journal:
Pediatr Nephrol
Journal subject:
NEFROLOGIA
/
PEDIATRIA
Year:
2011
Document type:
Article
Country of publication:
Germany