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Fragile X syndrome: Mechanistic insights and therapeutic avenues regarding the role of potassium channels
Fragile X syndrome (FXS) is a common form of mental disability and one of the known causes of autism. The mutation responsible for FXS is a large expansion of the trinucleotide CGG repeats which leads to DNA methylation of the fragile X mental retardation gene 1 (FMR1) and transcriptional silencing,...
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| Autors principals: | , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2012
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3393774/ https://ncbi.nlm.nih.gov/pubmed/22483378 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.conb.2012.03.010 |
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