A gain-of-function mutation in the CLCN2 chloride channel gene causes primary aldosteronism Nature Genetics volume 50, pages355–361 (2018)
Authors: Fabio L. Fernandes-Rosa, Georgios Daniil, Ian J. Orozco, Corinna Göppner, Rami El Zein, Vandana Jain, Sheerazed Boulkroun, Xavier Jeunemaitre, Laurence Amar, Hervé Lefebvre, Thomas Schwarzmayr, Tim M. Strom, Thomas J. Jentsch & Maria-Christina Zennaro doi:10.1038/s41588-018-0053-8
Scientific Coordinator: Dr Maria -Christina Zennaro, Head of INSERM U970 team 14: Genetic mechanisms of aldosterone-related disorders.
maria-christina.zennaro@inserm.fr
Project Manager (INSERM-Transfert): Kristina Fiedler
kristina.fiedler@inserm-transfert.fr
Paris Cardiovascular Research Center (PARCC), European Georges Pompidou Hospital, 56 rue Leblanc, 75015 Paris, France INSERM-Transfert, Paris Biopark, 7 rue Watt, 75013 Paris, France