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Cui X, Shu L, Liu B, Wang X, et al. Rare TGFBI Mutation c.1553T>G p.(L518R) in Lattice Corneal Dystrophy: Comprehensive Clinical and Genetic Analysis in a Chinese Family. Am J Ophthalmol 2025 Jul 14:S0002-9394(25)00366.
PMID: 40669590


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