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| A Korean Patient with Lattice Corneal Dystrophy Type IV with Leu527Arg Mutation in the |
| Jinsun Kim, Kyung A Lee, Eung Kweon Kim, Hyung Keun Lee |
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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  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 Novel mutation in the TGFBI gene in a patient with a late-onset lattice corneal dystrophy Acta Ophthalmologica. 2010;88:0-0 TGFBI gene mutation in a Chinese pedigree with Reis-Bücklers corneal dystrophy Ophthalmic and Physiological Optics. 2011;32(1):74-80 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 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 A case of lattice corneal dystrophy due to L527R mutation in the TGFBI gene with asymmetric corneal opacity in eye laterality Japanese Journal of Ophthalmology. 2010;54(6):628-629 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 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 A possible novel TGFBI mutation Ser591Phe in a Finnish family with lattice corneal dystrophy Acta Ophthalmologica. 2018;96(S261):55-56 |
