Identification of compound heterozygous KCNJ1 mutations (encoding ROMK) in a kindred with Bartter's syndrome and a functional analysis of their pathogenicity
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P. Welling | J. Sayer | K. Wood | S. Moochhala | M. Al-Hamed | A. Hynes | D. Reaich | Shalabh Srivastava | Dimin Li | Noel Edwards | A. C. Wroe