The Gitelman syndrome mutation, IVS9+1G>T, is common across Europe

Kidney Int. 2007 Oct;72(7):898. doi: 10.1038/sj.ki.5002504.
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • Europe
  • Founder Effect
  • Gitelman Syndrome / genetics*
  • Humans
  • Mutation
  • Receptors, Drug / genetics*
  • Roma / genetics*
  • Solute Carrier Family 12, Member 3
  • Symporters / genetics*

Substances

  • Receptors, Drug
  • SLC12A3 protein, human
  • Solute Carrier Family 12, Member 3
  • Symporters