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Genome-wide analysis validates aberrant methylation in fragile X syndrome is specific to the FMR1 locus
BACKGROUND: Fragile X syndrome (FXS) is a common form of inherited intellectual disability caused by an expansion of CGG repeats located in the 5(′) untranslated region (UTR) of the FMR1 gene, which leads to hypermethylation and silencing of this locus. Although a dramatic increase in DNA methylatio...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3599197/ https://ncbi.nlm.nih.gov/pubmed/23356558 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-14-18 |
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