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:
Online Access:http://scholarbank.nus.edu.sg/handle/10635/150853
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Institution: National University of Singapore
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