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Event-related potential alterations in fragile X syndrome

Fragile X Syndrome (FXS) is the most common form of X-linked intellectual disability (ID), associated with a wide range of cognitive and behavioral impairments. FXS is caused by a trinucleotide repeat expansion in the FMR1 gene located on the X-chromosome. FMR1 is expected to prevent the expression...

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Hlavní autoři: Knoth, Inga S., Lippé, Sarah
Médium: Artigo
Jazyk:Inglês
Vydáno: Frontiers Media S.A. 2012
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3449440/
https://ncbi.nlm.nih.gov/pubmed/23015788
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnhum.2012.00264
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