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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Detalhes bibliográficos
Main Authors: Olichney, John M., Chan, Shiaohui, Wong, Ling M., Schneider, Andrea, Seritan, Andreea, Niese, Adam, Yang, Jin-Chen, Laird, Kelsey, Teichholtz, Sara, Khan, Sara, Tassone, Flora, Hagerman, Randi
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2010
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Original Articles
Acesso em linha: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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