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Altered synaptic plasticity in a mouse model of fragile X mental retardation
Fragile X syndrome, the most common inherited form of human mental retardation, is caused by mutations of the Fmr1 gene that encodes the fragile X mental retardation protein (FMRP). Biochemical evidence indicates that FMRP binds a subset of mRNAs and acts as a regulator of translation. However, the...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The National Academy of Sciences
2002
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC124340/ https://ncbi.nlm.nih.gov/pubmed/12032354 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.122205699 |
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