Characterization of renal chloride channel (CLCN5) mutations in Dent's disease. by Yamamoto, K, Cox, J, Friedrich, T, Christie, P, Bald, M, Houtman, P, Lapsley, M, Patzer, L, Tsimaratos, M, Van'T Hoff, W, Yamaoka, K, Jentsch, T, Thakker, R

Adaptor protein-2 sigma subunit mutations causing familial hypocalciuric hypercalcaemia type 3 (FHH3) demonstrate genotype-phenotype correlations, codon bias and dominant-negative... by Hannan, F, Howles, S, Rogers, A, Cranston, T, Gorvin, C, Babinsky, V, Reed, A, Thakker, C, Bockenhauer, D, Brown, R, Connell, J, Cook, J, Darzy, K, Ehtisham, S, Graham, U, Hulse, T, Hunter, S, Izatt, L, Kumar, D, McKenna, M, McKnight, J, Morrison, P, Mughal, M, O'Halloran, D, Pearce, S, Porteous, M, Rahman, M, Richardson, T, Robinson, R, Scheers, I, Siddique, H, Van't Hoff, W, Wang, T, Whyte, M, Nesbit, M, Thakker, R