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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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Bibliografiske detaljer
Main Authors: Kim, So-Yeon, Hashimoto, Ryu-ichiro, Tassone, Flora, Simon, Tony J., Rivera, Susan M.
Format: Artigo
Sprog:Inglês
Udgivet: 2013
Fag:
Online adgang: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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