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An Atypical Phenotype of Macular and Peripapillary Retinal Atrophy Caused by a Mutation in the RP2 Gene
British Journal of Ophthalmology
- United Kingdom
doi 10.1136/bjo.2003.027979
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Categories
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Date
April 1, 2004
Authors
S S Dandekar
Publisher
BMJ
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