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Genetics and molecular pathology of Stargardt-like macular degeneration
Stargardt-like macular degeneration (STGD3) is an early onset, autosomal dominant macular degeneration. STGD3 is characterized by a progressive pathology, the loss of central vision, atrophy of the retinal pigment epithelium, and accumulation of lipofuscin, clinical features that are also characteri...
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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: |
2010
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3059896/ https://ncbi.nlm.nih.gov/pubmed/20096366 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.preteyeres.2010.01.001 |
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