Functional Characterization of Four Known Cav2.1 Variants Associated with Neurodevelopmental Disorders

por Folacci, Mathilde, Estaran, Sébastien, Ménard, Claudine, Bertaud, Anaïs, Rousset, Matthieu, Roussel, Julien, Thibaud, Jean-Baptiste, Vignes, Michel, Chavanieu, Alain, Charnet, Pierre, Cens, Thierry
Publicado 2023

Characterization of Loss-Of-Function KCNJ2 Mutations in Atypical Andersen Tawil Syndrome

por Le Tanno, Pauline, Folacci, Mathilde, Revilloud, Jean, Faivre, Laurence, Laurent, Gabriel, Pinson, Lucile, Amedro, Pascal, Millat, Gilles, Janin, Alexandre, Vivaudou, Michel, Roux-Buisson, Nathalie, Fauré, Julien
Publicado 2021