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Two mouse retinal degenerations caused by missense mutations in the beta-subunit of rod cGMP phosphodiesterase gene
We report the chromosomal localization, mutant gene identification, ophthalmic appearance, histology, and functional analysis of two new hereditary mouse models of retinal degeneration not having the Pde6b(rd1) (“r”, “rd”, or “rodless”) mutation. One strain harbors an autosomal recessive mutation th...
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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: |
2007
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2562796/ https://ncbi.nlm.nih.gov/pubmed/17267005 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.visres.2006.11.020 |
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