Study of Late-Onset Stargardt Type 1 Disease
Author:
Funder
Health Research Board
Health Research Charities Ireland
Foundation Fighting Blindness
Publisher
Elsevier BV
Subject
Ophthalmology
Reference44 articles.
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2. A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy;Allikmets;Nat Genet,1997
3. The spectrum of retinal phenotypes caused by mutations in the ABCA4 gene;Klevering;Graefes Arch Clin Exp Ophthalmol,2005
4. Early-onset Stargardt disease: phenotypic and genotypic characteristics;Lambertus;Ophthalmology,2015
5. ABCA4 midigenes reveal the full splice spectrum of all reported noncanonical splice site variants in Stargardt disease;Sangermano;Genome Res,2018
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