Lataa...
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...
Tallennettuna:
| Päätekijät: | , , , , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Society for Neuroscience
2010
|
| Aiheet: | |
| Linkit: | 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 |
| Tagit: |
Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!
|