An aquaporin-2 water channel mutant which causes autosomal dominant nephrogenic diabetes insipidus is retained in the Golgi complex.

  • S.M. Mulders
  • , D.G. Bichet
  • , J.P.L. Rijss
  • , E-J. Kamsteeg
  • , M-F. Arthus
  • , M. Lonergan
  • , M. Fujiwara
  • , K. Morgan
  • , R.L. Leijendekker
  • , P. van der Sluijs
  • , C.H. van Os
  • , P.M.T. Deen

Research output: Contribution to journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Pages (from-to)57-66
Number of pages10
JournalJournal of Clinical Investigation
Volume102
Publication statusPublished - 1998

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