Contrasting pathophysiological mechanisms of OPA1 mutations in autosomal dominant optic atrophy
Abstract Autosomal dominant optic atrophy (ADOA) caused by mutations in the nuclear-encoded OPA1 gene result in the preferential loss of retinal ganglion cells (RGCs) and progressive optic nerve degeneration. The severity of ADOA can be highly variable. This study compared the pathophysiological con...
| 出版年: | Cell Death Discovery |
|---|---|
| 主要な著者: | , , , , , , , , , , , , , , , , , |
| フォーマット: | 論文 |
| 言語: | 英語 |
| 出版事項: |
Nature Publishing Group
2025-05-01
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| オンライン・アクセス: | https://doi.org/10.1038/s41420-025-02442-8 |
