Mutations in Na(K)Cl transporters in Gitelman's and Bartter's syndromes

This publication has 26 references indexed in Scilit:

• Linkage of Infantile Bartter Syndrome with Sensorineural Deafness to Chromosome 1p
  American Journal of Human Genetics, 1998
• Mutations in the ROMK Gene in Antenatal Bartter Syndrome Are Associated with Impaired K+Channel Function
  Biochemical and Biophysical Research Communications, 1997
• Association of a mutation in thiazide-sensitive Na-Cl cotransporter with familial Gitelman's syndrome
  Journal of Clinical Endocrinology & Metabolism, 1996
• Gitelman’s syndrome is genetically distinct from other forms of Bartter’s syndrome
  Pediatric Nephrology, 1996
• Linkage of Gitelman syndrome to the thiazide-sensitive sodium-chloride cotransporter gene with identification of mutations in Dutch families
  Pediatric Nephrology, 1996
• Renal potassium channels: An overview
  Kidney International, 1995
• Bartter's syndrome: The unsolved puzzle
  American Journal of Kidney Diseases, 1995
• Cloning and expression of an inwardly rectifying ATP-regulated potassium channel
  Nature, 1993
• Renal Potassium Channels and Their Regulation
  Annual Review of Physiology, 1992
• Use of calcium excretion values to distinguish two forms of primary renal tubular hypokalemic alkalosis: Bartter and Gitelman syndromes
  The Journal of Pediatrics, 1992