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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Bibliographische Detailangaben
Hauptverfasser: 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
Sprache:Inglês
Veröffentlicht: Oxford University Press 2012
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Original Articles
Online Zugang: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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