Pseudohypoaldosteronism: mutation found, problem solved?

This publication has 29 references indexed in Scilit:

• Pseudohypo-aldosteronism and cholelithiasis: coincidence or pathogenetic correlation?
  European Journal of Pediatrics, 1997
• Localisation of Pseudohypoaldosteronism Genes to Chromosome 16p12.2–13.11 and 12p13.1-Pter by Homozygosity Mapping
  Human Molecular Genetics, 1996
• Pseudohypoaldosteronism: Family Studies to Identify Asymptomatic Carriers by Stimulation of the Renin-Aldosterone System
  Hormone Research, 1996
• Gitelman's variant of Barter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na–Cl cotransporter
  Nature Genetics, 1996
• Nephrocalcinosis in pseudohypoaldosteronism and the effect of indomethacin therapy
  The Journal of Pediatrics, 1994
• An Infant with Pseudohypoaldosteronism Accompanied by Cholelithiasis
  Neonatology, 1994
• The Epithelial Sodium Channel: Recent Developments
  Cellular Physiology and Biochemistry, 1993
• Pseudohypoaldosteronism in a preterm infant: Intrauterine presentation as hydramnios
  The Journal of Pediatrics, 1992
• Syndrome of hypertension and hyperkalemia with normal glomerular filtration rate.
  Hypertension, 1986
• Aldosterone-Receptor Deficiency in Pseudohypoaldosteronism
  New England Journal of Medicine, 1985