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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...
Autores principales: | Delprato, Anna, Xiao, Emily, Manoj, Devika |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
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 |
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