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A Korean Patient with Lattice Corneal Dystrophy Type IV with Leu527Arg Mutation in the TGFBI Gene
Jinsun Kim, Kyung A Lee, Eung Kweon Kim, Hyung Keun Lee
Korean J Ophthalmol. 2014;28(1):83-85.   Published online January 21, 2014
DOI: https://doi.org/10.3341/kjo.2014.28.1.83

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A Korean Patient with Lattice Corneal Dystrophy Type IV with Leu527Arg Mutation in theTGFBIGene
Korean Journal of Ophthalmology. 2014;28(1):83   Crossref logo
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A Novel Nonsense Mutation with a Compound Heterozygous Mutation in TGFBI Gene in Lattice Corneal Dystrophy Type I
Japanese Journal of Ophthalmology. 2003;47(1):13-17   Crossref logo
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Novel mutation in the TGFBI gene in a patient with a late-onset lattice corneal dystrophy
Acta Ophthalmologica. 2010;88:0-0   Crossref logo
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TGFBI gene mutation in a Chinese pedigree with Reis-B├╝cklers corneal dystrophy
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Lattice Corneal Dystrophy Type III in Patients with a Homozygous L527R Mutation in the TGFBI Gene
Japanese Journal of Ophthalmology. 2006;50(1):62-64   Crossref logo
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A Novel Variant of Combined Granular-Lattice Corneal Dystrophy Associated With the Met619Lys Mutation in the TGFBI Gene
Yearbook of Ophthalmology. 2009;2009:234-235   Crossref logo
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A case of lattice corneal dystrophy due to L527R mutation in the TGFBI gene with asymmetric corneal opacity in eye laterality
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Novel mutation (V505D) of the TGFBI gene found in a Chinese family with lattice corneal dystrophy, type I
Japanese Journal of Ophthalmology. 2005;49(2):84-88   Crossref logo
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De Novo L509P Mutation of the TGFBI Gene Associated with Slit-Lamp Findings of Lattice Corneal Dystrophy Type IIIA
Journal of Clinical Medicine. 2022;11(11):3055   Crossref logo
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A possible novel TGFBI mutation Ser591Phe in a Finnish family with lattice corneal dystrophy
Acta Ophthalmologica. 2018;96(S261):55-56   Crossref logo
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