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Fragile X–Associated Tremor/Ataxia Syndrome: Influence of the FMR1 Gene on Motor Fiber Tracts in Males With Normal and Premutation Alleles
IMPORTANCE: Individuals with the fragile X premutation express expanded CGG repeats (repeats 55–200) in the FMR1 gene and elevated FMR1 messenger RNA (mRNA) levels, both of which may underlie the occurrence of the late-onset neurodegenerative disorder fragile X–associated tremor/ataxia syndrome (FXT...
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| Hlavní autoři: | , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2013
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4028037/ https://ncbi.nlm.nih.gov/pubmed/23753897 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/jamaneurol.2013.2934 |
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