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

Journal of Clinical Investigation

Volumn 102, Issue 1, 1998, Pages 57-66

  Mulders, Sabine M ^a   Bichet, Daniel G ^b   Rijss, Johan P L ^a   Kamsteeg, Erik Jan ^a   Arthus, Marie Françoise ^b   Lonergan, Michele ^b   Fujiwara, Mary ^c   Morgan, Kenneth ^c   Leijendekker, Richtje ^d   Van Der Sluijs, Peter ^d   Van Os, Carel H ^a   Deen, Peter M T ^a  

^a RADBOUD UNIVERSITY NIJMEGEN   (Netherlands)

^b UNIVERSITÉ DE MONTRÉAL   (Canada)

^c MCGILL UNIVERSITY   (Canada)

^d UTRECHT UNIVERSITY   (Netherlands)

Author keywords

Aquaporin 2; Golgi apparatus; Mutation; Oocytes; Routing

Indexed keywords

AQUAPORIN;

ADULT; ALLELE; AMINO ACID SUBSTITUTION; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; ENDOPLASMIC RETICULUM; FEMALE; GENE MUTATION; GENETIC ANALYSIS; GOLGI COMPLEX; HUMAN; MULTIGENE FAMILY; NEPHROGENIC DIABETES INSIPIDUS; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN PHOSPHORYLATION; WATER TRANSPORT;

EID: 0032128360     PISSN: 00219738     EISSN: None     Source Type: Journal    
DOI: 10.1172/JCI2605     Document Type: Article

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