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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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Main Authors: | , , , , , , , , , , , |
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Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
BMJ Publishing Group
2014
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Assuntos: | |
Acesso em linha: | 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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