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Memory Deficits Due to Familial British Dementia BRI2 Mutation Are Caused by Loss of BRI2 Function Rather than Amyloidosis

Familial dementias, which include Alzheimer disease (AD), familial British dementia (FBD), and familial Danish dementia (FDD), are caused by dominantly inherited autosomal mutations and are characterized by the production of amyloidogenic peptides, neurofibrillary tangles (NFTs) and neurodegeneratio...

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Detalhes bibliográficos
Main Authors: Tamayev, Robert, Giliberto, Luca, Li, Wei, d'Abramo, Cristina, Arancio, Ottavio, Vidal, Ruben, D'Adamio, Luciano
Formato: Artigo
Idioma:Inglês
Publicado em: Society for Neuroscience 2010
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3056548/
https://ncbi.nlm.nih.gov/pubmed/21048150
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.3917-10.2010
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