Autosomal-Dominant Corneal Endothelial Dystrophies CHED1 and PPCD1 Are Allelic Disorders Caused by Non-coding Mutations in the Promoter of OVOL2. (2016)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2015.11.018
PubMed Identifier: 26749309
Publication URI: http://europepmc.org/abstract/MED/26749309
Type: Journal Article/Review
Volume: 98
Parent Publication: American journal of human genetics
Issue: 1
ISSN: 0002-9297