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Longitudinal Analysis of a Resolving Foveomacular Vitelliform Lesion in ABCA4 Disease

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By Winston Lee, Jana Zernant, Takayuki Nagasaki, Pei-Yin Su
| ophthalmologyretina.org
Allikmets R. Singh N. Sun H. Shroyer N.F. Hutchinson A. Chidambaram A. et al. A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy. Nat Genet. 1997; 15: 236-246 Cornelis S.S. Bax N.M. Zernant J. Allikmets R. Fritsche L.G. den Dunnen J.T. et al. Silico Functional Meta-Analysis of 5,962 ABCA4 Variants in 3,928 Retinal Dystrophy Cases. Hum Mutat. 2017; 38: 400-408 Cremers F.P.M. Lee W. Collin R.W.J. Allikmets R.
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