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