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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Détails bibliographiques
Auteurs principaux: Tamayev, Robert, Giliberto, Luca, Li, Wei, d'Abramo, Cristina, Arancio, Ottavio, Vidal, Ruben, D'Adamio, Luciano
Format: Artigo
Langue:Inglês
Publié: Society for Neuroscience 2010
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Articles
Accès en ligne: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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