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Marlhens, F., Bareil, C., Griffoin, JM. et al. Mutations in RPE65 cause Leber's congenital amaurosis. Nat Genet 17, 139–141 (1997). https://doi.org/10.1038/ng1097-139
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DOI: https://doi.org/10.1038/ng1097-139
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