Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations

The identification of a hexanucleotide repeat expansion in the C9ORF72 gene as the cause of chromosome 9-linked frontotemporal dementia and motor neuron disease offers the opportunity for greater understanding of the relationship between these disorders and other clinical forms of frontotemporal lob...

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Detalhes bibliográficos
Main Authors: Snowden, Julie S., Rollinson, Sara, Thompson, Jennifer C., Harris, Jennifer M., Stopford, Cheryl L., Richardson, Anna M. T., Jones, Matthew, Gerhard, Alex, Davidson, Yvonne S., Robinson, Andrew, Gibbons, Linda, Hu, Quan, DuPlessis, Daniel, Neary, David, Mann, David M. A., Pickering-Brown, Stuart M.
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2012
Assuntos:
Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3286329/
https://ncbi.nlm.nih.gov/pubmed/22300873
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/brain/awr355
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