A detailed phenotypic description of autosomal dominant cone dystrophy due to a de novo mutation in the GUCY2D gene. (2014)

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