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

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

10.1042/CS20130326

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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
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Institution: National University of Singapore

Internet

http://scholarbank.nus.edu.sg/handle/10635/150853

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