Phenotype of Three Consanguineous Tunisian Families With Early-Onset Retinal Degeneration Caused by an R91W Homozygous Mutation in the RPE65 Gene
Graefe's Archive for Clinical and Experimental Ophthalmology - Germany
doi 10.1007/s00417-005-0096-2
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Date
February 28, 2006
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Springer Nature