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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Detalhes bibliográficos
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2012
Assuntos:
Original Articles
Acesso em linha: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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