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An impaired routing of wild-type aquaporin-2 after tetramerization with an aquaporin-2 mutant explains dominant nephrogenic diabetes insipidus.

Autosomal recessive and dominant nephrogenic diabetes insipidus (NDI), a disease in which the kidney is unable to concentrate urine in response to vasopressin, are caused by mutations in the aquaporin-2 (AQP2) gene. Missense AQP2 proteins in recessive NDI have been shown to be retarded in the endopl...

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Detalhes bibliográficos
Main Authors: Kamsteeg, E J, Wormhoudt, T A, Rijss, J P, van Os, C H, Deen, P M
Formato: Artigo
Idioma:Inglês
Publicado em: 1999
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1171322/
https://ncbi.nlm.nih.gov/pubmed/10228154
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/emboj/18.9.2394
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