📣 Help Shape the Future of UKRI's Gateway to Research (GtR)

We're improving UKRI's Gateway to Research and are seeking your input! If you would be interested in being interviewed about the improvements we're making and to have your say about how we can make GtR more user-friendly, impactful, and effective for the Research and Innovation community, please email gateway@ukri.org.

Detection of mutations in KLHL3 and CUL3 in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome) (2014)

First Author: Glover M

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

Parent Publication: Clinical Science

Issue: 10

ISSN: 0143-5221