Associated Papers
Nasal Retinal Degeneration Is a Feature of a Subset of CRX-Associated Retinopathies.
Massengill MT et al.
Genes, 2026
Clinical spectrum, genetic complexity and therapeutic approaches for retinal disease caused by ABCA4 mutations.
Cremers FPM et al.
Progress in Retinal and Eye Research, 2020
Utility of a Genetic Screening Panel in Patients With Suspected Inherited Retinal Dystrophies.
McGowan H et al.
Ophthalmic Surgery, Lasers & Imaging Retina, 2020
Pathogenicity discrimination and genetic test reference for CRX variants based on genotype-phenotype analysis.
Yi Z et al.
Experimental Eye Research, 2019
Quantitative fundus autofluorescence distinguishes ABCA4-associated and non-ABCA4-associated bull's-eye maculopathy.
Duncker T et al.
Ophthalmology, 2015
A drosophila genetic resource of mutants to study mechanisms underlying human genetic diseases.
Yamamoto S et al.
Cell, 2014
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