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Abnormal N400 word repetition effects in fragile X-associated tremor/ataxia syndrome
Fragile X-associated tremor/ataxia syndrome, a neurodegenerative disorder associated with premutation alleles (55–200 CGG repeats) of the FMR1 gene, affects many carriers in late-life. Patients with fragile X-associated tremor/ataxia syndrome typically have cerebellar ataxia, intranuclear inclusions...
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| Hoofdauteurs: | , , , , , , , , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Oxford University Press
2010
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2859155/ https://ncbi.nlm.nih.gov/pubmed/20410144 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/brain/awq077 |
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