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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Détails bibliographiques
Auteurs principaux: 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.
Format: Artigo
Langue:Inglês
Publié: Oxford University Press 2012
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Original Articles
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC3286330/
https://ncbi.nlm.nih.gov/pubmed/22366791
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/brain/awr361
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