Photoreceptor-induced RPE phagolysosomal maturation defects in Stargardt-like Maculopathy (STGD3)
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-018-24357-4.pdf
Reference51 articles.
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2. Grayson, C. & Molday, R. S. Dominant negative mechanism underlies autosomal dominant Stargardt-like macular dystrophy linked to mutations in ELOVL4. J. Biol. Chem. 280, 32521–32530 (2005).
3. Barabas, P. et al. Role of ELOVL4 and very long-chain polyunsaturated fatty acids in mouse models of Stargardt type 3 retinal degeneration. Proc. Natl. Acad. Sci. USA 110, 5181–5186 (2013).
4. Kuny, S., Gaillard, F. & Sauvé, Y. Differential gene expression in eyecup and retina of a mouse model of Stargardt-like macular dystrophy (STGD3). Invest. Ophthalmol. Vis. Sci. 53, 664–675 (2012).
5. Logan, S. et al. Deciphering mutant ELOVL4 activity in autosomal-dominant Stargardt macular dystrophy. Proc. Natl. Acad. Sci. USA 110, 5446–5451 (2013).
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