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Biochimica Et Biophysica Acta. Molecular Basis of Disease|August 16, 2017
A novel PMCA3 mutation in an ataxic patient with hypomorphic phosphomannomutase 2 (PMM2) heterozygote mutations: Biochemical characterization of the pump defectMattia Vicario, Tito Calì, Domenico Cieri, et al.Biochimica Et Biophysica Acta. Molecular Basis of Disease|September 16, 2016
The ataxia related G1107D mutation of the plasma membrane Ca2+ ATPase isoform 3 affects its interplay with calmodulin and the autoinhibition processTito Calì, Martina Frizzarin, Laura Luoni, et al.Neurobiology of Disease|April 16, 2018
A V1143F mutation in the neuronal-enriched isoform 2 of the PMCA pump is linked with ataxiaMattia Vicario, Ginevra Zanni, Francesca Vallese, et al.Cell Death & Disease|October 7, 2022
The ataxia-linked E1081Q mutation affects the sub-plasma membrane Ca2+-microdomains by tuning PMCA3 activityFrancesca Vallese, Lorenzo Maso, Flavia Giamogante, et al.Pageof 4