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Toward Fulfilling the Promise of Molecular Medicine in Fragile X Syndrome
Fragile X syndrome (FXS) is the most common inherited form of mental retardation and a leading known cause of autism. It is caused by loss of expression of the fragile X mental retardation protein (FMRP), an RNA-binding protein that negatively regulates protein synthesis. In neurons, multiple lines...
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| Huvudupphovsmän: | , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
2011
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| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3100156/ https://ncbi.nlm.nih.gov/pubmed/21090964 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1146/annurev-med-061109-134644 |
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