Detection of mutations in KLHL3 and CUL3 in families with fhht (familial hyperkalaemic hypertension or gordon's syndrome)

10.1042/CS20130326

Saved in:

Bibliographic Details
Main Authors:	Glover M., Ware J.S., Henry A., Wolley M., Walsh R., Wain L.V., Xu S., Hoff W.G.V., Tobin M.D., Hall I.P., Cook S., Gordon R.D., Stowasser M., O'shaughnessy K.M.
Other Authors:	DUKE-NUS MEDICAL SCHOOL
Format:	Article
Published:	2019
Subjects:	Diuretic Gordon's syndrome Hyperkalaemia Hypertension Pseudohypoaldosteronism Thiazide
Online Access:	http://scholarbank.nus.edu.sg/handle/10635/150853
Tags:	Add Tag No Tags, Be the first to tag this record!
Institution:	National University of Singapore

id	sg-nus-scholar.10635-150853
record_format	dspace
spelling	sg-nus-scholar.10635-1508532023-09-21T08:18:34Z Detection of mutations in KLHL3 and CUL3 in families with fhht (familial hyperkalaemic hypertension or gordon's syndrome) Glover M. Ware J.S. Henry A. Wolley M. Walsh R. Wain L.V. Xu S. Hoff W.G.V. Tobin M.D. Hall I.P. Cook S. Gordon R.D. Stowasser M. O'shaughnessy K.M. DUKE-NUS MEDICAL SCHOOL Diuretic Gordon's syndrome Hyperkalaemia Hypertension Pseudohypoaldosteronism Thiazide 10.1042/CS20130326 Clinical Science 126 10 721-726 CSCIA 2019-01-15T08:25:49Z 2019-01-15T08:25:49Z 2014 Article Glover M., Ware J.S., Henry A., Wolley M., Walsh R., Wain L.V., Xu S., Hoff W.G.V., Tobin M.D., Hall I.P., Cook S., Gordon R.D., Stowasser M., O'shaughnessy K.M. (2014). Detection of mutations in KLHL3 and CUL3 in families with fhht (familial hyperkalaemic hypertension or gordon's syndrome). Clinical Science 126 (10) : 721-726. ScholarBank@NUS Repository. https://doi.org/10.1042/CS20130326 1435221 http://scholarbank.nus.edu.sg/handle/10635/150853 Scopus
institution	National University of Singapore
building	NUS Library
continent	Asia
country	Singapore Singapore
content_provider	NUS Library
collection	ScholarBank@NUS
topic	Diuretic Gordon's syndrome Hyperkalaemia Hypertension Pseudohypoaldosteronism Thiazide
spellingShingle	Diuretic Gordon's syndrome Hyperkalaemia Hypertension Pseudohypoaldosteronism Thiazide Glover M. Ware J.S. Henry A. Wolley M. Walsh R. Wain L.V. Xu S. Hoff W.G.V. Tobin M.D. Hall I.P. Cook S. Gordon R.D. Stowasser M. O'shaughnessy K.M. Detection of mutations in KLHL3 and CUL3 in families with fhht (familial hyperkalaemic hypertension or gordon's syndrome)
description	10.1042/CS20130326
author2	DUKE-NUS MEDICAL SCHOOL
author_facet	DUKE-NUS MEDICAL SCHOOL Glover M. Ware J.S. Henry A. Wolley M. Walsh R. Wain L.V. Xu S. Hoff W.G.V. Tobin M.D. Hall I.P. Cook S. Gordon R.D. Stowasser M. O'shaughnessy K.M.
format	Article
author	Glover M. Ware J.S. Henry A. Wolley M. Walsh R. Wain L.V. Xu S. Hoff W.G.V. Tobin M.D. Hall I.P. Cook S. Gordon R.D. Stowasser M. O'shaughnessy K.M.
author_sort	Glover M.
title	Detection of mutations in KLHL3 and CUL3 in families with fhht (familial hyperkalaemic hypertension or gordon's syndrome)
title_short	Detection of mutations in KLHL3 and CUL3 in families with fhht (familial hyperkalaemic hypertension or gordon's syndrome)
title_full	Detection of mutations in KLHL3 and CUL3 in families with fhht (familial hyperkalaemic hypertension or gordon's syndrome)
title_fullStr	Detection of mutations in KLHL3 and CUL3 in families with fhht (familial hyperkalaemic hypertension or gordon's syndrome)
title_full_unstemmed	Detection of mutations in KLHL3 and CUL3 in families with fhht (familial hyperkalaemic hypertension or gordon's syndrome)
title_sort	detection of mutations in klhl3 and cul3 in families with fhht (familial hyperkalaemic hypertension or gordon's syndrome)
publishDate	2019
url	http://scholarbank.nus.edu.sg/handle/10635/150853
_version_	1778168969831645184

Detection of mutations in KLHL3 and CUL3 in families with fhht (familial hyperkalaemic hypertension or gordon's syndrome)

Similar Items