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CRX controls retinal expression of the X-linked juvenile retinoschisis (RS1) gene

X-linked juvenile retinoschisis is a heritable condition of the retina in males caused by mutations in the RS1 gene. Still, the cellular function and retina-specific expression of RS1 are poorly understood. To address the latter issue, we characterized the minimal promoter driving expression of RS1...

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書誌詳細
主要な著者: Langmann, Thomas, Lai, Christine C. L., Weigelt, Karin, Tam, Beatrice M., Warneke-Wittstock, Regina, Moritz, Orson L., Weber, Bernhard H. F.
フォーマット: Artigo
言語:Inglês
出版事項: Oxford University Press 2008
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC2582616/
https://ncbi.nlm.nih.gov/pubmed/18927113
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkn737
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