FOXP2 down expression is associated with executive dysfunctions and electrophysiological abnormalities of brain in Autism spectrum disorder; a neuroimaging genetic study

BACKGROUND AND AIMS: Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by language impairment, and challenges with social interaction, communication, and repetitive behaviors. Although genetics are a primary cause of ASD, the exact genes and molecular mechanisms involved...

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Detalles Bibliográficos
Autores principales: Haghighatfard, Arvin, Yaghoubi asl, Elham, Bahadori, Rosita Azar, Aliabadian, Rojina, Farhadi, Mahdi, Mohammadpour, Fatemeh, Tabrizi, Zeinab
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9620679/
https://www.ncbi.nlm.nih.gov/pubmed/36382065
http://dx.doi.org/10.1177/23969415221126391

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9620679/
https://www.ncbi.nlm.nih.gov/pubmed/36382065
http://dx.doi.org/10.1177/23969415221126391

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