Mathilde Folacci

发表

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

M. Vignes, J. Thibaud, P. Charnet, 2023, Membranes.

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

L. Faivre, J. Fauré, G. Millat, 2021, Frontiers in Genetics.

Multiple combinations of RDL subunits diversify the repertoire of GABA receptors in the honey bee parasite Varroa destructor

M. Vignes, J. Thibaud, P. Charnet, 2018, The Journal of Biological Chemistry.