Aggregation-prone GFAP mutation in Alexander disease validated using a zebrafish model
Abstract Background Alexander disease (AxD) is an astrogliopathy that predominantly affects the white matter of the central nervous system (CNS), and is caused by a mutation in the gene encoding the glial fibrillary acidic protein (GFAP), an intermediate filament primarily expressed in astrocytes an...
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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: |
BMC
2017-09-01
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| シリーズ: | BMC Neurology |
| 主題: | |
| オンライン･アクセス: | http://link.springer.com/article/10.1186/s12883-017-0938-7 |
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