Read our latest related publication online:
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
This project has received funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement No 633983
Scientific Coordinator: Dr Maria -Christina Zennaro, Head of INSERM U970 team 14: Genetic mechanisms of aldosterone-related disorders. [email protected]
Project Manager (INSERM-Transfert): Catherine Clusel [email protected]
Project Manager (INSERM-Transfert): Kristina Fiedler [email protected]
More contact details here
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