Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type IIIDavid B. Simon, Richard P. Lifton, Érica Mendonça et al.|Nature Genetics|1997Cited by 869
Genetic heterogeneity of Barter's syndrome revealed by mutations in the K+ channel, ROMKDavid B. Simon, Richard P. Lifton, Fiona E. Karet et al.|Nature Genetics|1996Cited by 824