A detailed phenotypic description of autosomal dominant cone dystrophy due to a de novo mutation in the GUCY2D gene. (2014)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1038/eye.2014.7
PubMed Identifier: 24480840
Publication URI: http://europepmc.org/abstract/MED/24480840
Type: Journal Article/Review
Volume: 28
Parent Publication: Eye (London, England)
Issue: 4
ISSN: 0950-222X