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Amyloid and intracellular accumulation of BRI(2)
Familial British dementia (FBD) and familial Danish dementia (FDD) are caused by mutations in the BRI(2) gene. These diseases are characterized clinically by progressive dementia and ataxia and neuropathologically by amyloid deposits and neurofibrillary tangles. Herein, we investigate BRI(2) protein...
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| Vydáno v: | Neurobiol Aging |
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| Hlavní autoři: | , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2016
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5359036/ https://ncbi.nlm.nih.gov/pubmed/28131015 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neurobiolaging.2016.12.018 |
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