Commonalities and distinctions between two neurodevelopmental disorder subtypes associated with SCN2A and SCN8A variants and literature review - Mangano, Giuseppe Donato; Fontana, Antonina; Antona, Vincenzo; Salpietro, Vincenzo; Mangano, Giuseppa Renata; Giuffrè, Mario; Nardello, Rosaria (Molecular genetics & genomic medicine, 2022)
Keywords: Age; Autism; Autism Spectrum Disorder - genetics; autism spectrum disorders; Channels; Clinical Report; Clinical Reports; Convulsions & seizures; Disorders; EEG; Epilepsy; Epilepsy - genetics; Genetic diversity; Genetic variance; Genotype & phenotype; Humans; Intellectual disabilities; intellectual disability; Intellectual Disability - genetics; Literature reviews; Memory; Mutation; NAV1.2 Voltage-Gated Sodium Channel - genetics; NAV1.6 Voltage-Gated Sodium Channel - genetics; Neurodevelopmental disorders; Neurodevelopmental Disorders - genetics; Neuropsychology; Observational studies; Observational Studies as Topic; Patients; Phenotype; Phenotypes; SCN2A; SCN8A; Sodium channels (voltage-gated); Standard scores; whole‐exome sequencing; Italy; epilepsy; EEG; SCN8A; autism spectrum disorders; SCN2A; whole-exome sequencing; intellectual disability