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Detection of mutations in KLHL3 and CUL3 in families with Familial Hyperkalaemic Hypertension (FHH or Gordon syndrome). (2014)

First Author: Wolley 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

Type: Conference/Paper/Proceeding/Abstract

Volume: 63, No 6 June 2014, e160

Parent Publication: Published in Hypertension. Australian High Blood Pressure Research Council Annual Scientific Meeting, Melbourne, Australia

Issue: 6 e160