A Study on the CLCN5 Gene in Iranian Patients: A Report of Novel and Recurrent Mutations

Conclusion: This is the first report to characterize mutations in theCLCN5 gene in Iranian patients with Dent ’s disease and expands the spectrum ofCLCN5 mutations by reporting two novel mutations, c.1241_1242dupAA and c.805-2A#x3e;G.Nephron
Source: Nephron - Category: Urology & Nephrology Source Type: research