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Autosomal dominant stromal corneal dystrophy associated with a SPARCL1 missense variant (2024)

First Author: Braddock F

Attributed to: Gene regulation, genetic mechanisms and development of potential therapies for corneal endothelial dystrophies funded by UKRI FLF

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/s41431-024-01687-8

Publication URI: http://dx.doi.org/10.1038/s41431-024-01687-8

Type: Journal Article/Review

Parent Publication: European Journal of Human Genetics

Issue: 12