Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleThe Gitelman syndrome mutation, IVS9+1G>T, is common across Europe.AuthorsBouwer, S. T.; Coto, E.; Santos, F.; Angelicheva, D.; Chandler, D.; Kalaydjieva, L.AbstractA letter to the editor is presented in response to the article "A new mutation (intron 9 +1 G>T) in the SLC12A3 gene is linked to Gitelman syndrome in Gypsies," by E. Coto and colleagues in a previous issue.SubjectsLETTERS to the editor; GENETIC mutationPublicationKidney International, 2007, Vol 72, Issue 7, p898ISSN0085-2538Publication typeLetterDOI10.1038/sj.ki.5002504