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Autor:
Ilektra Kouranti, Rosa Vargas-Poussou, Gerardo Gamba, Marguerite Hureaux, Richard Grimm, Eric Clauser, Robert J. Unwin, Tiffany Migeon, Nirubiah Thurairajasingam, Marcio Do Cruzeiro, Richard A. Coleman, Chloé Rafael, Eduardo R. Argaiz, Xavier Jeunemaitre, Kevin O’Shaugnessy, Stéphanie Baron, Hélène Louis-Dit-Picard, Ivan Tack, Juliette Hadchouel, María Chávez-Canales, Paolo Mulatero, Paul A. Welling, Waed Abdel-Khalek, Xavier Girerd, Stéphane Decramer, Irmine Loisel-Ferreira, Olivier Staub, Sarah Vacle, Gwenaelle Roussey
Publikováno v:
J Clin Invest
Journal of Clinical Investigation
Journal of Clinical Investigation, 2020, 130 (12), pp.6379-6394. ⟨10.1172/JCI94171⟩
Journal of Clinical Investigation
Journal of Clinical Investigation, 2020, 130 (12), pp.6379-6394. ⟨10.1172/JCI94171⟩
International audience; Gain-of-function mutations in with no lysine (K) 1 (WNK1) and WNK4 genes are responsible for familial hyperkalemic hypertension (FHHt), a rare, inherited disorder characterized by arterial hypertension and hyperkalemia with me