Primary hyperoxaluria type 1 with a novel mutation.
Indian J Pediatr
; 2009 Feb; 76(2): 215-7
Article
в En
| IMSEAR
| ID: sea-79666
Полный текст:
1
База данных:
IMSEAR
Основная тема:
Hyperoxaluria, Primary
/
Female
/
Humans
/
Male
/
Calcium Oxalate
/
Point Mutation
/
Galactosyltransferases
/
Infant
/
Kidney
/
Nephrocalcinosis
Язык:
En
Журнал:
Indian J Pediatr
Год:
2009
Тип:
Article