Visual Function in Children with GNAO1-Related Encephalopathy

Visual Function in Children with GNAO1-Related Encephalopathy

Background: GNAO1-related encephalopathies include a broad spectrum of developmental disorders caused by de novo heterozygous mutations in the GNAO1 gene, encoding the G (o) subunit α of G-proteins. These conditions are characterized by epilepsy, movement disorders and developmental impairment, in c...

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Bibliographic Details
Main Authors: Maria Luigia Gambardella, Elisa Pede, Lorenzo Orazi, Simona Leone, Michela Quintiliani, Giulia Maria Amorelli, Maria Petrianni, Marta Galanti, Filippo Amore, Elisa Musto, Marco Perulli, Ilaria Contaldo, Chiara Veredice, Eugenio Maria Mercuri, Domenica Immacolata Battaglia, Daniela Ricci
Format: Article
Language:English
Published: MDPI AG 2023-02-01
Series:Genes
Subjects:
neurovisual competences
GNAO1 mutation
visual function
Online Access:https://www.mdpi.com/2073-4425/14/3/544

Internet

https://www.mdpi.com/2073-4425/14/3/544

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