Associated Papers
CTNNA1-associated retinal dystrophy: novel multimodal imaging and electrophysiology features.
Alexis JA et al.
Documenta Ophthalmologica. Advances in Ophthalmology, 2025
40455352 (PubMed )
Supplement: 10633_2025_10027_MOESM1_ESM.pdf
Clinical and Genetic Findings in CTNNA1-Associated Macular Pattern Dystrophy.
Tanner A et al.
Ophthalmology, 2021
Catenin α 1 mutations cause familial exudative vitreoretinopathy by overactivating Norrin/β-catenin signaling.
Zhu X et al.
The Journal of Clinical Investigation, 2021
Identification of Possible Risk Variants of Familial Strabismus Using Exome Sequencing Analysis.
An JY et al.
Genes, 2021
Mutations in CTNNA1 cause butterfly-shaped pigment dystrophy and perturbed retinal pigment epithelium integrity.
Saksens NT et al.
Nature Genetics, 2016
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