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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Bibliographic Details
Published in:	Dementia and Geriatric Cognitive Disorders Extra
Main Authors:	Anna-Lotta Kaivorinne, Michaela K. Bode, Liisa Paavola, Hannu Tuominen, Mika Kallio, Alan E. Renton, Bryan J. Traynor, Virpi Moilanen, Anne M. Remes
Format:	Article
Language:	English
Published:	Karger Publishers 2013-08-01
Subjects:	Association study Clinical features Frontotemporal dementia Frontotemporal lobar degeneration Genetics
Online Access:	http://www.karger.com/Article/FullText/351859

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