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Perry Syndrome: A Distinctive Type of TDP-43 Proteinopathy
Perry syndrome is a rare atypical parkinsonism with depression, apathy, weight loss, and central hypoventilation caused by mutations in dynactin p150(glued) (DCTN1). A rare distal hereditary motor neuropathy, HMN7B, also has mutations in DCTN1. Perry syndrome has TAR DNA-binding protein of 43 kDa (T...
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| 出版年: | J Neuropathol Exp Neurol |
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| 主要な著者: | , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2017
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5901076/ https://ncbi.nlm.nih.gov/pubmed/28789478 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/jnen/nlx049 |
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