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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Autors principals: Kaivorinne, Anna-Lotta, Bode, Michaela K., Paavola, Liisa, Tuominen, Hannu, Kallio, Mika, Renton, Alan E., Traynor, Bryan J., Moilanen, Virpi, Remes, Anne M.
Format: Artigo
Idioma:Inglês
Publicat: S. Karger AG 2013
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Original Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3776392/
https://ncbi.nlm.nih.gov/pubmed/24052799
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000351859
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