Author:
Yang Guoxing,Liu Zhiqiang,Xie Shipeng,Li Chengquan,Lv Lina,Zhang Minglian,Zhao Jialiang
Publisher
Springer Science and Business Media LLC
Reference26 articles.
1. Lauber, H. Die sogenannte Retinitis Punctata Albescens. Klin Monatsbl Augenheilkd. 48, 133–48 (1910).
2. Yamamoto, H. et al. Mutations in the gene encoding 11-cis retinol dehydrogenase cause delayed dark adaptation and fundus albipunctatus. Nat Genet. 22, 188–91 (1999).
3. Kiser, P. D., Golczak, M., Maeda, A. & Palczewski, K. Key enzymes of the retinoid (visual) cycle in vertebrate retina. Biochim Biophys Acta. 1821, 137-51 (2012).
4. Gu, S. M. et al. Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophy. Nat Genet. 17, 194–7 (1997).
5. Morimura, H. et al. Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or Leber congenital amaurosis. Proc Natl Acad Sci USA 95, 3088–93 (1998).
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