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NEW EMBO MEMBER’S REVIEW: On the genetics of retinitis pigmentosa and on mutation-independent approaches to therapeutic intervention
Retinitis pigmentosa (RP), the group of hereditary conditions involving death of retinal photoreceptors, represents the most prevalent cause of visual handicap among working populations in developed countries. Here we provide an overview of the molecular pathologies associated with such disorders, f...
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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: |
Oxford University Press
2002
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC125887/ https://ncbi.nlm.nih.gov/pubmed/11867514 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/emboj/21.5.857 |
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