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Altered neural activity of magnitude estimation processing in adults with the fragile X premutation
Mutations of the fragile X mental retardation 1 (FMR1) gene are the genetic cause of fragile X syndrome (FXS). Expanded CGG trinucleotide repeat (> 200 repeats) result in transcriptional silencing of the FMR1 gene and deficiency/absence of the FMR1 protein (FMRP). Carriers with a premutation alle...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3880247/ https://ncbi.nlm.nih.gov/pubmed/24045061 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jpsychires.2013.08.014 |
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