A novel mutation in the GRHPR gene in a Japanese patient with primary hyperoxaluria type 2.
Takayama T, Nagata M, Ozono S, Nonomura K, Cramer SD. A novel mutation in the GRHPR gene in a Japanese patient with primary hyperoxaluria type 2. Nephrol Dial Transplant. 2007 Aug; 22(8):2371-4.