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Comprehensive Motor Testing in Fmr1-KO Mice Exposes Temporal Defects in Oromotor Coordination
Fragile X syndrome (FXS; MIM #300624), a well-recognized form of inherited human mental retardation is caused, in most cases, by a CGG trinucleotide repeat expansion in the 5′-untranslated region of FMR1, resulting in reduced expression of the fragile X mental retardation protein (FMRP). Clinical fe...
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| Vydáno v: | Behav Neurosci |
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| Hlavní autoři: | , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2011
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4874324/ https://ncbi.nlm.nih.gov/pubmed/22004265 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1037/a0025920 |
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