Fundus autofluorescence imaging in hereditary retinal diseases

Author:

Pichi Francesco1ORCID,Abboud Emad B.1,Ghazi Nicola G.1,Khan Arif O.1

Affiliation:

1. Eye Institute; Cleveland Clinic Abu Dhabi; Abu Dhabi United Arab Emirates

Publisher

Wiley

Subject

Ophthalmology,General Medicine

Reference66 articles.

1. Enhanced accumulation of A2E in individuals homozygous or heterozygous for mutations in BEST1 (VMD2);Bakall;Exp Eye Res,2007

2. Autosomal recessive bestrophinopathy: differential diagnosis and treatment options;Boon;Ophthalmology,2013

3. The formation of autofluorescent granules in cultured human RPE;Boulton;Invest Ophthalmol Vis Sci,1989

4. North Carolina macular dystrophy (MCDR1) caused by a novel tandem duplication of the PRDM13 gene;Bowne;Mol Vis,2016

5. Fundus autofluorescence of choroidal nevi and melanoma;Cennamo;Acta Ophthalmol,2017

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