The W258X mutation in SLC22A is the predominant cause of Japanese renal hypouricemia.
Bibliographic Information
- Title
- The W258X mutation in SLC22A is the predominant cause of Japanese renal hypouricemia.
- Author
- komoda F, Igarashi T, et al.
Journal
-
- Pediatr Nephrol 19(5)
-
Pediatr Nephrol 19(5) 728-733, 2004
