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Phenotype of Autosomal Dominant Cone–rod Dystrophy Due to the R838C Mutation of the GUCY2D Gene Encoding Retinal Guanylate Cyclase-1
Eye
- United Kingdom
doi 10.1038/sj.eye.6702612
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Abstract
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Categories
Medicine
Arts
Sensory Systems
Ophthalmology
Humanities
Date
October 13, 2006
Authors
M Smith
N Whittock
A Searle
M Croft
C Brewer
M Cole
Publisher
Springer Science and Business Media LLC
