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Congenital progressive hydronephrosis (cph) is caused by an S256L mutation in aquaporin-2 that affects its phosphorylation and apical membrane accumulation.

Authors
Type
Published Article
Journal
Proceedings of the National Academy of Sciences of the United States of America
Publication Date
Volume
103
Issue
18
Pages
6952–6957
Identifiers
PMID: 16641094
Source
Medline

Abstract

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