Liddle Syndrome: Review of the Literature and Description of a New Case

Liddle syndrome is an inherited form of low-renin hypertension, transmitted with an autosomal dominant pattern. The molecular basis of Liddle syndrome resides in germline mutations of the SCNN1A, SCNN1B and SCNN1G genes, encoding the α, β, and γ-subunits of the epithelial Na(+) channel (ENaC), respe...

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Publicat a:Int J Mol Sci
Autors principals: Tetti, Martina, Monticone, Silvia, Burrello, Jacopo, Matarazzo, Patrizia, Veglio, Franco, Pasini, Barbara, Jeunemaitre, Xavier, Mulatero, Paolo
Format: Artigo
Idioma:Inglês
Publicat: MDPI 2018
Matèries:
Review
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5877673/
https://ncbi.nlm.nih.gov/pubmed/29534496
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms19030812
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