Amélie Cordovado

Équipe : Translational research in neurogenetic diseases (NRGEN)
Post-doctorante  |  UB

Publications

Heterozygous Missense Variants in the ATPase Phospholipid Transporting 9A Gene, ATP9A, Alter Dendritic Spine Maturation and Cause Dominantly Inherited Nonsyndromic Intellectual Disability
Amélie Cordovado, Yvan Hérenger, Coline Cormier, Estrella López-Martín, Hannah Stamberger, Laurence Faivre, Anne-Sophie Denommé-Pichon, Antonio Vitobello, Hamza Hadj Abdallah, Giulia Barcia, Thomas Courtin, Beatriz Martínez-Delgado, Eva Bermejo-Sánchez, María J. Barrero, Brooklynn Gasser, Stéphane Bezieau, Sébastien Küry, Sarah Weckhuysen, Frédéric Laumonnier, Annick Toutain, Marie-Laure Vuillaume
Human Mutation. 2025-01-01
10.1155/humu/7085599