Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: evidence for genetic heterogeneity. International Collaborative Study Group for Bartter-like Syndromes [published erratum appears in Hum Mol Genet 1997 Apr;6(4):650]Lothar Károlyi, Steven Hébert, D Zimmermann et al.|Human Molecular Genetics|1997Cited by 190
Antenatal Bartter syndrome with sensorineural deafness: refinement of the locus on chromosome 1p31Martin Vollmer, Nine Knoers, Nikola Jeck et al.|Nephrology Dialysis Transplantation|2000Cited by 26