Novel disease-causing variants and phenotypic features of X-linked megalocornea. (2022)
Attributed to:
Gene regulation, genetic mechanisms and development of potential therapies for corneal endothelial dystrophies
funded by
FLF
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1111/aos.15022
PubMed Identifier: 34644435
Publication URI: http://europepmc.org/abstract/MED/34644435
Type: Journal Article/Review
Volume: 100
Parent Publication: Acta ophthalmologica
Issue: 4
ISSN: 1755-375X