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Corneal Dystrophy, Lattice Type IIIA

Known as: CDL3A, Lattice Corneal Dystrophy, Type IIIA 
National Institutes of Health

Related topics

Related topics

4 relations
Autosomal dominant inheritanceCorneal erosionFamilial Amyloid Polyneuropathy, Type V

Broader (1)

Hereditary corneal dystrophy

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2016
Review
2016
Delayed Onset of Lattice Corneal Dystrophy Type IIIA Due to a Novel T621P Mutation in TGFBI.
To the Editor: We recently identified a family with lattice corneal dystrophy type IIIA (LCD IIIA) associated with a novel… 
2011
2011
Genotype-phenotype correlations in Chinese patients with TGFBI gene-linked corneal dystrophy
In this paper, we report the clinical and molecular features of the distinct TGFBI (human transforming growth factor β-induced… 
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