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Pathological mechanisms underlying TDP-43 driven neurodegeneration in FTLD–ALS spectrum disorders
Aggregation of misfolded TAR DNA-binding protein 43 (TDP-43) is a striking hallmark of neurodegenerative processes that are observed in several neurological disorders, and in particular in most patients diagnosed with frontotemporal lobar degeneration (FTLD) or amyotrophic lateral sclerosis (ALS). A...
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| 主要な著者: | , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2013
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3782069/ https://ncbi.nlm.nih.gov/pubmed/23900071 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddt349 |
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