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Phenotype and genotype of concurrent keratoconus and Fuchs endothelial corneal dystrophy. (2023)

First Author: Liu S

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

PubMed Identifier: 36883248

Publication URI: http://europepmc.org/abstract/MED/36883248

Type: Journal Article/Review

Volume: 101

Parent Publication: Acta ophthalmologica

Issue: 6

ISSN: 1755-375X