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Degeneration of dopaminergic neurons and impaired intracellular trafficking in Atp13a2 deficient zebrafish
ATP13A2 is the autosomal recessive causative gene for juvenile-onset Parkinson’s disease (PARK9, Parkinson’s disease 9), also known as Kufor-Rakeb syndrome. The disease is characterized by levodopa-responsive Parkinsonism, supranuclear gaze palsy, spasticity, and dementia. Previously, we have report...
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| 出版年: | IBRO Rep |
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| 主要な著者: | , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Elsevier
2020
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7283103/ https://ncbi.nlm.nih.gov/pubmed/32529115 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ibror.2020.05.002 |
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