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Zhang, Kang | New locus for autosomal dominant stargardt-like disease maps to chromosome 4 | Stargardt disease (STGD) is the most common hereditary macular dystrophy and is characterized by decreased central vision, atrophy of the macula and underlying retinal-pigment epithelium, and frequent presence of prominent flecks in the posterior pole of the retina. STGD is most commonly inherited a... | Haplotypes; Genetic Markers | 1999 |
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