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Article

A late-onset unilateral variant of lattice corneal dystrophy not associated with a TGFBI mutation.

The British journal of ophthalmology - 1 Mar 2008

Yellore V S, Sonmez B, Rayner S A, Aldave A J

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Share to Corneal Dystrophies, Hereditary
Share to TGFBI gene
Share to Mutation
Share to Transforming Growth Factor beta1

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 18303168
DOI: 10.1136/bjo.2007.120352

Genes

TGFBI

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

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A late-onset unilateral variant of lattice corneal dystrophy not associated with a TGFBI mutation.PMID 18303168Read ↗

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Late-onset Form of Lattice Corneal Dystrophy Caused by Leu527Arg Mutation of the TGFBI GeneSemantic proximity Read ↗

Variant lattice corneal dystrophy associated with compound heterozygous mutations in the TGFBI gene.Semantic proximity Read ↗

Lattice corneal dystrophy type IIIA with hyaline component from a novel A620P mutation and distinct surgical treatments.Semantic proximity Read ↗

Lattice corneal dystrophy associated with the Ala546Asp and Pro551Gln missense changes in the TGFBI geneSemantic proximity Read ↗

A mutation within exon 14 of the TGFBI (BIGH3) gene on chromosome 5q31 causes an asymmetric, late-onset form of lattice corneal dystrophySemantic proximity Read ↗

Clinical and genetic aspects of the TGFBI-associated corneal dystrophies.Semantic proximity Read ↗

Anterior basement membrane corneal dystrophy and pseudo-unilateral lattice corneal dystrophy in a patient with recurrent corneal erosions.Semantic proximity Read ↗

A Korean patient with lattice corneal dystrophy type IV with Leu527Arg mutation in the TGFBI gene.Semantic proximity Read ↗

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