Fig. 2From: Dent-2 disease with a Bartter-like phenotype caused by the Asp631Glu mutation in the OCRL geneFamily tree and segregation analysis for the Asp631Glu mutation of OCRL1. Family members were examined for the Asp631Glu mutation; two males and two females were affected. Males presented the whole spectrum of Dent-2 disease. Female carriers presented only phosphaturia. LMWP: low molecular weight proteinuriaBack to article page