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

The study of families with rare inherited forms of hypo- and hyper-tension has been one of the most successful strategies to probe the molecular pathophysiology of blood pressure control and has revealed dysregulation of distal nephron Na(+) reabsorption to be a common mechanism. FHHt (familial hype...

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Detaylı Bibliyografya
Asıl Yazarlar: Glover, Mark, Ware, James S., Henry, Amanda, Wolley, Martin, Walsh, Roddy, Wain, Louise V., Xu, Shengxin, Van’t Hoff, William G., Tobin, Martin D., Hall, Ian P., Cook, Stuart, Gordon, Richard D., Stowasser, Michael, O’Shaughnessy, Kevin M.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Portland Press Ltd. 2014
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Original Paper
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3963521/
https://ncbi.nlm.nih.gov/pubmed/24266877
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/CS20130326
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