Cognitive Assessment in GNAO1 Neurodevelopmental Disorder Using an Eye Tracking System

GNAO1 gene mutations are associated with a neurodevelopmental disorder characterized by developmental delay, epilepsy, and movement disorder. Eye tracking and eye movement analysis are an intriguing method to assess cognitive and language function and, to the best of our knowledge, it has never been...

Descripción completa

Detalles Bibliográficos
Autores principales: Graziola, Federica, Garone, Giacomo, Grasso, Melissa, Capuano, Alessandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8397136/
https://www.ncbi.nlm.nih.gov/pubmed/34441836
http://dx.doi.org/10.3390/jcm10163541

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8397136/
https://www.ncbi.nlm.nih.gov/pubmed/34441836
http://dx.doi.org/10.3390/jcm10163541

Ejemplares similares