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- A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy Journal Article
- A new locus for autosomal dominant Stargardt-like disease maps to chromosome 4 Journal Article
- A new locus for dominant drusen and macular degeneration maps to chromosome 6q14 Journal Article
- A novel mutation in the ABCR gene in four patients with autosomal recessive Stargardt disease Journal Article
- A therapeutic aptamer inhibits angiogenesis by specifically targeting the heparin binding domain of VEGF165 Journal Article
- Clinical and genetic studies of an autosomal dominant cone-rod dystrophy with features of Stargardt disease. Journal Article
- DICER1 deficit induces Alu RNA toxicity in age-related macular degeneration Journal Article
- ERK1/2 activation is a therapeutic target in age-related macular degeneration Journal Article
- The ABCR gene in recessive and dominant Stargardt diseases: A genetic pathway in macular degeneration Journal Article