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...

Descripción completa

Detalles Bibliográficos
Autores principales: Kaivorinne, Anna-Lotta, Bode, Michaela K., Paavola, Liisa, Tuominen, Hannu, Kallio, Mika, Renton, Alan E., Traynor, Bryan J., Moilanen, Virpi, Remes, Anne M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2013
Materias:
Original Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3776392/
https://www.ncbi.nlm.nih.gov/pubmed/24052799
http://dx.doi.org/10.1159/000351859

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3776392/
https://www.ncbi.nlm.nih.gov/pubmed/24052799
http://dx.doi.org/10.1159/000351859

Ejemplares similares