Temporal Requirements of the Fragile X Mental Retardation Protein in Modulating Circadian Clock Circuit Synaptic Architecture

Loss of fragile X mental retardation 1 (FMR1) gene function is the most common cause of inherited mental retardation and autism spectrum disorders, characterized by attention disorder, hyperactivity and disruption of circadian activity cycles. Pursuit of effective intervention strategies requires de...

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Detalles Bibliográficos
Autores principales: Gatto, Cheryl L., Broadie, Kendal
Formato: Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2009
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2737437/
https://www.ncbi.nlm.nih.gov/pubmed/19738924
http://dx.doi.org/10.3389/neuro.04.008.2009

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2737437/
https://www.ncbi.nlm.nih.gov/pubmed/19738924
http://dx.doi.org/10.3389/neuro.04.008.2009

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