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The Time Course of Deafness and Retinal Degeneration in a Kunming Mouse Model for Usher Syndrome
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Dominant Retinitis Pigmentosa, p.Gly56Arg Mutation in NR2E3: Phenotype in a Large Cohort of 24 Cases
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Mutation Detection in Patients with Retinal Dystrophies Using Targeted Next Generation Sequencing
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