Phenotype and genotype of concurrent keratoconus and Fuchs endothelial corneal dystrophy (2023)
Attributed to:
Triplet repeat expansion-associated inherited corneal disease: from genetic mechanism to clinical consequences
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1111/aos.15654
Publication URI: http://dx.doi.org/10.1111/aos.15654
Type: Journal Article/Review
Parent Publication: Acta Ophthalmologica
Issue: 6