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Altered neural activity in the `when' pathway during temporal processing in fragile X premutation carriers
Mutations of the fragile X mental retardation 1 (FMR1) gene are the genetic cause of fragile X syndrome (FXS). Large expansions of the CGG repeat (>200 repeats) consequently result in transcriptional silencing of the FMR1 gene and deficiency/absence of the FMR1 protein (FMRP). Carriers with a pre...
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| Publicado no: | Behav Brain Res |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4867552/ https://ncbi.nlm.nih.gov/pubmed/24398265 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bbr.2013.12.044 |
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