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See Latest ArticlesThe Natural History of Stargardt Disease with Specific Sequence Mutation in the ABCA4 Gene
Investigative Ophthalmology and Visual Science, 07/08/09
Genead MA et al. - In these patients with Stargardt disease and a Gly1961Glu mutation, the majority showed a clinical phenotype characterized by fundus changes localized to the foveal and parafoveal region, normal ERG amplitudes, absence of a silent or masked choroid, and a mean age of initial presentation in the third decade.
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