Connecting DCX, COMT and FMR1 in social behavior and cognitive impairment

Genetic variants of DCX, COMT and FMR1 have been linked to neurodevelopmental disorders related to intellectual disability and social behavior. In this systematic review we examine the roles of the DCX, COMT and FMR1 genes in the context of hippocampal neurogenesis with respect to these disorders wi...

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Detalles Bibliográficos
Autores principales: Delprato, Anna, Xiao, Emily, Manoj, Devika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9121553/
https://www.ncbi.nlm.nih.gov/pubmed/35590332
http://dx.doi.org/10.1186/s12993-022-00191-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9121553/
https://www.ncbi.nlm.nih.gov/pubmed/35590332
http://dx.doi.org/10.1186/s12993-022-00191-7

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