Familial frontotemporal dementia with neuronal intranuclear inclusions is not a polyglutamine expansion disease

BACKGROUND: Many cases of frontotemporal dementia (FTD) are familial, often with an autosomal dominant pattern of inheritance. Some are due to a mutation in the tau- encoding gene, on chromosome 17, and show an accumulation of abnormal tau in brain tissue (FTDP-17T). Most of the remaining familial c...

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Detalhes bibliográficos
Main Authors: Mackenzie, Ian R, Butland, Stefanie L, Devon, Rebecca S, Dwosh, Emily, Feldman, Howard, Lindholm, Caroline, Neal, Scott J, Ouellette, BF Francis, Leavitt, Blair R
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2006
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1570137/
https://ncbi.nlm.nih.gov/pubmed/16945149
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2377-6-32
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