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A Mutation in ZNF513, a Putative Regulator of Photoreceptor Development, Causes Autosomal-Recessive Retinitis Pigmentosa
Authors:Lin Li  Naoki Nakaya  Venkata RM Chavali  Zhiwei Ma  Paul A Sieving  Stanislav I Tomarev  S Amer Riazuddin  J Fielding Hejtmancik
Institution:1 Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA
2 Section of Molecular Mechanisms of Glaucoma, Laboratory of Molecular and Developmental Biology, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA
3 National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA
4 State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-Sen University, 54 Xianlie Road, Guangzhou 510060, China
5 Department of Ophthalmology, University of California San Diego, Jacobs Retina Center, #206, La Jolla, CA 92037, USA
6 National Centre of Excellence in Molecular Biology, University of the Punjab, Lahore-53700, Pakistan
7 Allama Iqbal Medical College, Lahore-54550, Pakistan
8 The Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA
Abstract:
Keywords:
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