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Altered body schema processing in frontotemporal dementia with C9ORF72 mutations

BACKGROUND: Mutations in C9ORF72 are an important cause of frontotemporal dementia (FTD) and motor neuron disease. Accumulating evidence suggests that FTD associated with C9ORF72 mutations (C9ORF72-FTD) is distinguished clinically by early prominent neuropsychiatric features that might collectively...

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Bibliografische gegevens
Hoofdauteurs: Downey, Laura E, Fletcher, Phillip D, Golden, Hannah L, Mahoney, Colin J, Agustus, Jennifer L, Schott, Jonathan M, Rohrer, Jonathan D, Beck, Jonathan, Mead, Simon, Rossor, Martin N, Crutch, Sebastian J, Warren, Jason D
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: BMJ Publishing Group 2014
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Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4145454/
https://ncbi.nlm.nih.gov/pubmed/24521566
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jnnp-2013-306995
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