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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...
Gorde:
| Argitaratua izan da: | Behav Brain Res |
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| Egile Nagusiak: | , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
2014
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| Gaiak: | |
| Sarrera elektronikoa: | 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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