Showing 1 - 2 results of 2 for search 'Van'T Hoff, W', query time: 0.02s
Refine Results
-
1
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
Published 2000Journal article -
2
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
Published 2015Journal article