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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