Clinical Characteristics of C9ORF72-Linked Frontotemporal Lobar Degeneration

Background: The most common genetic cause of frontotemporal lobar degeneration (FTLD) and amyotrophic lateral sclerosis (ALS) has been linked to a hexanucleotide repeat expansion in the C9ORF72 gene. The frequency of the C9ORF72 expansion in Finland is among the highest in the world. Methods: We ass...

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Veröffentlicht in:	Dementia and geriatric cognitive disorders extra 2013-08, Vol.3 (1), p.251-262
Hauptverfasser:	Kaivorinne, Anna-Lotta, Bode, Michaela K., Paavola, Liisa, Tuominen, Hannu, Kallio, Mika, Renton, Alan E., Traynor, Bryan J., Moilanen, Virpi, Remes, Anne M.
Format:	Artikel
Sprache:	eng
Schlagworte:	Association study Clinical features Frontotemporal dementia Frontotemporal lobar degeneration Genetics Original Original Research Article
Online-Zugang:	Volltext
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