Widening the infantile hypotonia with psychomotor retardation and characteristic Facies-1 Syndrome’s clinical and molecular spectrum through NALCN in-silico structural analysis - Vecchio, Davide; Macchiaiolo, Marina; Gonfiantini, Michaela V.; Panfili, Filippo M.; Petrizzelli, Francesco; Liorni, Niccolò; Cortellessa, Fabiana; Sinibaldi, Lorenzo; Rana, Ippolita; Agolini, Emanuele; Cocciadiferro, Dario; Colantoni, Nicole; et al. (Frontiers in Genetics, 2024)