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Author

A. V. Cideciyan

2 papers indexed here

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Review Aug 2026

Unique retinal phenotype may support pathogenicity of FSCN2 in inherited retinal degenerations: a case report and review of the literature

ABSTRACT Purpose To describe a peculiar retinal phenotype associated with a novel variant in FSCN2. Methods The patient underwent a comprehensive ophthalmic exam, imaging with spectral domain optical coherence tomography (SD-OCT) and fundus autofluorescence and vision measured with kinetic fields and full-field electro...

C. Sherman, A. Sumaroka, Alejandro J. Roman et al. · 1 citation

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