论文信息 - Identification of compound heterozygous KCNJ1 mutations (encoding ROMK) in a kindred with Bartter's syndrome and a functional analysis of their pathogenicity - 字舞流文

Identification of compound heterozygous KCNJ1 mutations (encoding ROMK) in a kindred with Bartter's syndrome and a functional analysis of their pathogenicity

P. Welling | J. Sayer | K. Wood | S. Moochhala | M. Al-Hamed | A. Hynes | D. Reaich | Shalabh Srivastava | Dimin Li | Noel Edwards | A. C. Wroe