Gandini, M. A., Souza, I. A., Ferron, L., Innes, A. M., & Zamponi, G. W. (2021). The de novo CACNA1A pathogenic variant Y1384C associated with hemiplegic migraine, early onset cerebellar atrophy and developmental delay leads to a loss of Cav2.1 channel function. Mol Brain.

Gandini, Maria A., Ivana A. Souza, Laurent Ferron, A. Micheil Innes, و Gerald W. Zamponi. "The De Novo CACNA1A Pathogenic Variant Y1384C Associated With Hemiplegic Migraine, Early Onset Cerebellar Atrophy and Developmental Delay Leads to a Loss of Cav2.1 Channel Function." Mol Brain 2021.

Gandini, Maria A., et al. "The De Novo CACNA1A Pathogenic Variant Y1384C Associated With Hemiplegic Migraine, Early Onset Cerebellar Atrophy and Developmental Delay Leads to a Loss of Cav2.1 Channel Function." Mol Brain 2021.