Highlighting the Dystonic Phenotype Related to GNAO1 - Wirth, Thomas; Garone, Giacomo; Kurian, Manju A.; Piton, Amélie; Millan, Francisca; Telegrafi, Aida; Drouot, Nathalie; Rudolf, Gabrielle; Chelly, Jamel; Marks, Warren; Burglen, Lydie; Demailly, Diane; et al. (Movement disorders, 2022)
Keywords: Basal ganglia; Central nervous system diseases; Chorea; Dystonia; Dystonia - genetics; Dystonic Disorders; Dystonic Disorders - genetics; Encephalopathy; Epilepsy; Genetics; Genotype & phenotype; GNAO1; GTP-Binding Protein alpha Subunits, Gi-Go - genetics; GTP-Blinding Protein alpha Subinits, Gi-Go; Humans; Intellectual disabilities; Life Sciences; Movement Disorders; Movement Disorders - genetics; mutation; Myoclonus; Neurons and Cognition; Parkinsonian Disorders; Parkinsonian Disorders - genetics; Patients; Phenotype; Phenotypes; GNAO1; mutation; phenotypes; dystonia; Phenotypes; Mutation; Dystonia