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pro vyhledávání: '"Patrizia Matarazzo"'
Autor:
Martina Tetti, Silvia Monticone, Jacopo Burrello, Patrizia Matarazzo, Franco Veglio, Barbara Pasini, Xavier Jeunemaitre, Paolo Mulatero
Publikováno v:
International Journal of Molecular Sciences, Vol 19, Iss 3, p 812 (2018)
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-s
Externí odkaz:
https://doaj.org/article/1d2267d6dea3449891dbf5ff40b4e88f
Autor:
Patrizia Matarazzo, Martina Tetti, Xavier Jeunemaitre, Jacopo Burrello, Silvia Monticone, Barbara Pasini, Franco Veglio, Paolo Mulatero
Publikováno v:
International Journal of Molecular Sciences, Vol 19, Iss 3, p 812 (2018)
International Journal of Molecular Sciences
International Journal of Molecular Sciences
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-s