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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Hlavní autoři: 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.
Médium: Artigo
Jazyk:Inglês
Vydáno: Oxford University Press 2012
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Original Articles
On-line přístup: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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