Detection of mutations in KLHL3 and CUL3 in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome). (2014)
Attributed to:
Genetic and molecular characterisation of sodium reabsorption by thiazide-sensitive pathways in the kidney
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1042/cs20130326
PubMed Identifier: 24266877
Publication URI: http://europepmc.org/abstract/MED/24266877
Type: Journal Article/Review
Volume: 126
Parent Publication: Clinical science (London, England : 1979)
Issue: 10
ISSN: 0143-5221