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Reevaluation of FMR1 Hypermethylation Timing in Fragile X Syndrome
Fragile X syndrome (FXS) is one of the most common heritable forms of cognitive impairment. It results from a fragile X mental retardation protein (FMRP) protein deficiency caused by a CGG repeat expansion in the 5′-UTR of the X-linked FMR1 gene. Whereas in most individuals the number of CGGs is ste...
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| Publicado no: | Front Mol Neurosci |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Frontiers Media S.A.
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5808132/ https://ncbi.nlm.nih.gov/pubmed/29467618 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnmol.2018.00031 |
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