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Freund, C., Wang, QL., Chen, S. et al. De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis. Nat Genet 18, 311–312 (1998). https://doi.org/10.1038/ng0498-311
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DOI: https://doi.org/10.1038/ng0498-311
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