An aquaporin-2 water channel mutant which causes autosomal dominant nephrogenic diabetes insipidus is retained in the Golgi complex.
S.M. Mulders(Radboud University Nijmegen), Peter M.T. Deen(Radboud University Nijmegen), Richtje Leijendekker(Utrecht University), Peter van der Sluijs(Utrecht University), Daniel G. Bichet(Hôpital du Sacré-Cœur de Montréal), Erik‐Jan Kamsteeg(Radboud University Nijmegen), Kenneth Morgan(University of London), Michèle Lonergan(Hôpital du Sacré-Cœur de Montréal), C.H. van Os(University of Zurich), Masasuke Fujiwara(Pediatrics and Genetics), Marie‐Françoise Arthus(Hôpital du Sacré-Cœur de Montréal), J.P.L. Rijss(Radboud University Nijmegen)
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