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Investigating FUS variation in Parkinson’s disease
Mutations of the FUS gene were first reported to cause amyotrophic lateral sclerosis (ALS). Subsequent studies confirmed the role of mutations in ALS and also implicated them in frontotemporal dementia (FTD). Recently, through Next-Generation Exome sequencing approaches a mutation resulting in a sub...
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| 出版年: | Parkinsonism Relat Disord |
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| 主要な著者: | , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2014
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4721223/ https://ncbi.nlm.nih.gov/pubmed/24262168 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/S1353-8020(13)70035-X |
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