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A mouse model of the fragile X premutation: effects on behavior, dendrite morphology, and regional rates of cerebral protein synthesis
Carriers of FMR1 premutation alleles have 55–200 CGG repeats in the 5’ untranslated region of the gene. These individuals are at risk for fragile X associated primary ovarian insufficiency (females) and, in late life, fragile X associated tremor and ataxia syndrome (males, and to a lesser extent, fe...
Tallennettuna:
| Päätekijät: | , , , , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2011
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3150744/ https://ncbi.nlm.nih.gov/pubmed/21220020 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2011.01.008 |
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