The ABCR Gene in Recessive and Dominant Stargardt Diseases: A Genetic Pathway in Macular Degeneration
Author:
Publisher
Elsevier BV
Subject
Genetics
Reference10 articles.
1. A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy;Allikmets;Nat. Genet.,1997
2. Mutation of the Stargardt disease gene (ABCR) in age-related macular degeneration;Allikmets;Science,1997
3. Age-related macular degeneration;Bressler;Surv. Ophthalmol.,1988
4. Autosomal recessive retinitis pigmentosa and cone–rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCR;Cremers;Hum. Mol. Genet.,1998
5. A gene for Stargardt's disease (fundus flavimaculatus) maps to the short arm of chromosome 1;Kaplan;Nat. Genet.,1993
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