North Carolina macular dystrophy (MCDR1)
Author:
Publisher
Informa UK Limited
Subject
Genetics(clinical),Ophthalmology,Pediatrics, Perinatology, and Child Health
Link
http://www.tandfonline.com/doi/pdf/10.3109/13816819309042913
Reference21 articles.
1. Hereditary Macular Degeneration and Amino-Aciduria
2. A New Dominant Progressive Foveal Dystrophy
3. Gass J DM. Stereoscopic Atlas of Macular Diseases, 3rd edn. CV Mosby, St Louis 1987; 98–99
4. Central Areolar Pigment Epithelial Dystrophy (With 1 color plate)
5. Central Areolar Pigment Epithelial Dystrophy
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1. Comments on “The possible pathogenesis of macular caldera in patients with North Carolina macular dystrophy”;BMC Ophthalmology;2023-09-08
2. Responding to comments on “The possible pathogenesis of macular caldera in patients with North Carolina macular dystrophy.“;BMC Ophthalmology;2023-09-08
3. Report on the 2021 Aniridia North America symposium on PAX6, aniridia, and beyond;The Ocular Surface;2023-07
4. Letter to the Editor Regarding: "Modern diagnostic and therapeutic approaches in familial maculopathy with reference to North Carolina macular dystrophy" by Jana Nekolova et al.;Biomedical Papers;2023-03-15
5. New Noncoding Base Pair Mutation at the Identical Locus as the Original NCMD/MCDR1 in a Mexican Family, Suggesting a Mutational Hotspot;Journal of VitreoRetinal Diseases;2023-01
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