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Multiple Mechanisms Contribute to Leakiness of a Frameshift Mutation in Canine Cone-Rod Dystrophy
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MSH3-Deficiency Initiates EMAST without Oncogenic Transformation of Human Colon Epithelial Cells
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Expression of Wild-Type Rp1 Protein in Rp1 Knock-in Mice Rescues the Retinal Degeneration Phenotype
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Prevalence and Clinical Features of Hearing Loss Patients with CDH23 Mutations: A Large Cohort Study
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