Should Patients with Kearns-Sayre Syndrome and Corneal Endothelial Failure Be Genotyped for a TCF4 Trinucleotide Repeat, Commonly Associated with Fuchs Endothelial Corneal Dystrophy? (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/genes12121918
PubMed Identifier: 34946867
Publication URI: http://europepmc.org/abstract/MED/34946867
Type: Journal Article/Review
Volume: 12
Parent Publication: Genes
Issue: 12
ISSN: 2073-4425