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

<h4>Background</h4>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.<h4>Obje...

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Bibliografski detalji

Glavni autori:	Eino Solje, Heidi Aaltokallio, Heli Koivumaa-Honkanen, Noora M Suhonen, Virpi Moilanen, Anna Kiviharju, Bryan Traynor, Pentti J Tienari, Päivi Hartikainen, Anne M Remes
Format:	Artigo
Jezik:	Inglês
Izdano:	Public Library of Science (PLoS) 2015-01-01
Serija:	PLoS ONE
Online pristup:	https://doi.org/10.1371/journal.pone.0131817
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