Author:
Yeboah Gyening Kofi,Lobanova Ekaterina S.,Brush Richard S.,Agbaga Martin-Paul
Funder
Oklahoma Center for the Advancement of Science and Technology
National Institutes of Health
Knights Templar Eye Foundation
Presbyterian Health Foundation
Research to Prevent Blindness
BrightFocus Foundation
Subject
Cell Biology,Endocrinology,Biochemistry
Reference188 articles.
1. A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy;Zhang;Nat. Genet.,2001
2. A novel gene for autosomal dominant Stargardt-like macular dystrophy with homology to the SUR4 protein family;Edwards;Invest. Ophthalmol. Vis. Sci.,2001
3. Diverse macular dystrophy phenotype caused by a novel complex mutation in the ELOVL4 gene;Bernstein;Invest. Ophthalmol. Vis. Sci.,2001
4. A novel mutation in the ELOVL4 gene causes autosomal dominant Stargardt-like macular dystrophy;Maugeri;Invest. Ophthalmol. Vis. Sci.,2004
5. Lipofuscin redistribution and loss accompanied by cytoskeletal stress in retinal pigment epithelium of eyes with age-related macular degeneration;Ach;Invest. Ophthalmol. Vis. Sci.,2015
Cited by
45 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献