Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features

An expanded hexanucleotide repeat in the C9ORF72 gene has recently been identified as a major cause of familial frontotemporal lobar degeneration and motor neuron disease, including cases previously identified as linked to chromosome 9. Here we present a detailed retrospective clinical, neuroimaging...

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Detalles Bibliográficos
Autores principales: Mahoney, Colin J., Beck, Jon, Rohrer, Jonathan D., Lashley, Tammaryn, Mok, Kin, Shakespeare, Tim, Yeatman, Tom, Warrington, Elizabeth K., Schott, Jonathan M., Fox, Nick C., Rossor, Martin N., Hardy, John, Collinge, John, Revesz, Tamas, Mead, Simon, Warren, Jason D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2012
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3286330/
https://www.ncbi.nlm.nih.gov/pubmed/22366791
http://dx.doi.org/10.1093/brain/awr361

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3286330/
https://www.ncbi.nlm.nih.gov/pubmed/22366791
http://dx.doi.org/10.1093/brain/awr361

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