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Zanni G et al.Mutation of plasma membrane Ca2+ ATPase isoform 3 in a family with X-linked congenital cerebellar ataxia impairs Ca2+ homeostasis. Proc Natl Acad Sci U S A. 2012;109(36):14514-9. PMID: 22912398
Calì T et al.A Novel Mutation in Isoform 3 of the Plasma Membrane Ca2+ Pump Impairs Cellular Ca2+ Homeostasis in a Patient with Cerebellar Ataxia and Laminin Subunit 1α Mutations. J Biol Chem. 2015;290(26):16132-41. PMID: 25953895
Feyma T et al.Dystonia in ATP2B3-associated X-linked spinocerebellar ataxia. Mov Disord. 2016;31(11):1752-1753. PMID: 27653636
Vicario M et al.A novel PMCA3 mutation in an ataxic patient with hypomorphic phosphomannomutase 2 (PMM2) heterozygote mutations: Biochemical characterization of the pump defect. Biochim Biophys Acta Mol Basis Dis. 2017;1863(12):3303-3312. PMID: 28807751
Zanni G et al.Mutation of plasma membrane Ca2+ ATPase isoform 3 in a family with X-linked congenital cerebellar ataxia impairs Ca2+ homeostasis. Proc Natl Acad Sci U S A. 2012;109(36):14514-9. PMID: 22912398