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Rescue of behavioral phenotype and neuronal protrusion morphology in Fmr1 KO mice
Lack of fragile X mental retardation protein (FMRP) causes Fragile X Syndrome, the most common form of inherited mental retardation. FMRP is an RNA-binding protein and is a component of messenger ribonucleoprotein complexes, associated with brain polyribosomes, including dendritic polysomes. FMRP is...
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| Main Authors: | , , , , , , , |
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| Format: | Artigo |
| Language: | Inglês |
| Published: |
2008
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| Subjects: | |
| Online Access: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2481236/ https://ncbi.nlm.nih.gov/pubmed/18571098 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2008.04.002 |
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