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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Bibliografiska uppgifter
Huvudupphovsmän: Tamayev, Robert, Giliberto, Luca, Li, Wei, d'Abramo, Cristina, Arancio, Ottavio, Vidal, Ruben, D'Adamio, Luciano
Materialtyp: Artigo
Språk:Inglês
Publicerad: Society for Neuroscience 2010
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Articles
Länkar: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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