Non-Penetrance for Ocular Phenotype in Two Individuals Carrying Heterozygous Loss-of-Function ZEB1 Alleles. (2021)
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/10.3390/genes12050677
PubMed Identifier: 33946386
Publication URI: http://europepmc.org/abstract/MED/33946386
Type: Journal Article/Review
Volume: 12
Parent Publication: Genes
Issue: 5
ISSN: 2073-4425