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Fragile X and autism: Intertwined at the molecular level leading to targeted treatments
Fragile X syndrome (FXS) is caused by an expanded CGG repeat (> 200 repeats) in the 5' untranslated portion of the fragile mental retardation 1 gene (FMR1), leading to deficiency or absence of the FMR1 protein (FMRP). FMRP is an RNA carrier protein that controls the translation of several ot...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2954865/ https://ncbi.nlm.nih.gov/pubmed/20858229 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/2040-2392-1-12 |
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