The Phenotype of the C9ORF72 Expansion Carriers According to Revised Criteria for bvFTD

BACKGROUND: The C9ORF72 expansion is one of the most common genetic etiologies observed with behavioural variant frontotemporal dementia (bvFTD). Revised diagnostic criteria for bvFTD (FTDC) were recently introduced but only a few studies have evaluated the accuracy of these criteria. OBJECTIVE: The...

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Vydáno v:PLoS One
Hlavní autoři: Solje, Eino, Aaltokallio, Heidi, Koivumaa-Honkanen, Heli, Suhonen, Noora M., Moilanen, Virpi, Kiviharju, Anna, Traynor, Bryan, Tienari, Pentti J., Hartikainen, Päivi, Remes, Anne M.
Médium: Artigo
Jazyk:Inglês
Vydáno: Public Library of Science 2015
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Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4493025/
https://ncbi.nlm.nih.gov/pubmed/26146826
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0131817
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