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SPATA7: Evolving Phenotype from Cone-Rod Dystrophy to Retinitis Pigmentosa
BACKGROUND: SPATA7 mutations have been associated with different autosomal recessive retinal degeneration phenotypes. Long-term follow-up has not been described in detail. MATERIALS AND METHODS: A Hispanic patient with SPATA7 mutations was evaluated serially over a 12-year period with kinetic and st...
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| 出版年: | Ophthalmic Genet |
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| 主要な著者: | , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2016
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4988809/ https://ncbi.nlm.nih.gov/pubmed/26854980 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3109/13816810.2015.1130154 |
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