ロード中...
The Prevalence and Natural History of Dominant Optic Atrophy due to OPA1 Mutations
PURPOSE: Autosomal dominant optic atrophy (DOA) is a major cause of visual impairment in young adults and it is characterized by selective retinal ganglion cell loss. In order to define the prevalence and natural history of this optic nerve disorder, we performed a population-based epidemiological a...
保存先:
| 主要な著者: | , , , , , , , , , , , |
|---|---|
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2010
|
| 主題: | |
| オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4040407/ https://ncbi.nlm.nih.gov/pubmed/20417570 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ophtha.2009.12.038 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|