Characterisation of the Cullin-3 mutation that causes a severe form of familial hypertension and hyperkalaemia

Published 2015 View Full Article

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Title
Characterisation of the Cullin-3 mutation that causes a severe form of familial hypertension and hyperkalaemia
Authors
Keywords
-
Journal
EMBO Molecular Medicine
Volume 7, Issue 10, Pages 1285-1306
Publisher
EMBO
Online
2015-08-19
DOI
10.15252/emmm.201505444

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