Cargando...
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...
Gardado en:
| Publicado en: | Behav Brain Res |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
2014
|
| Assuntos: | |
| Acceso en liña: | 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 |
| Tags: |
Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!
|