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

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  • Additional Information
    • Source:
      Publisher: Elsevier Country of Publication: United States NLM ID: 0323470 Publication Model: Print Cited Medium: Print ISSN: 0085-2538 (Print) Linking ISSN: 00852538 NLM ISO Abbreviation: Kidney Int Subsets: MEDLINE
    • Publication Information:
      Publication: 2016- : New York : Elsevier
      Original Publication: New York, Springer-Verlag.
    • Subject Terms:
      Gitelman Syndrome/*genetics ; Receptors, Drug/*genetics ; Roma/*genetics ; Symporters/*genetics; Europe ; Founder Effect ; Humans ; Mutation ; Solute Carrier Family 12, Member 3
    • Comments:
      Comment on: Kidney Int. 2004 Jan;65(1):25-9. doi: 10.1111/j.1523-1755.2004.00388.x. (PMID: 14675033)
    • Accession Number:
      0 (Receptors, Drug)
      0 (SLC12A3 protein, human)
      0 (Solute Carrier Family 12, Member 3)
      0 (Symporters)
    • Publication Date:
      Date Created: 20070921 Date Completed: 20071219 Latest Revision: 20151119
    • Publication Date:
      20250114
    • Accession Number:
      10.1038/sj.ki.5002504
    • Accession Number:
      17882248