Work

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

Year: 2026

Type: article

Study design: Case Report

Source: Ophthalmic Genetics

DOI: 10.1080/13816810.2026.2717331

Authors: Caroline L. Sherman, Alexander Sumaroka, Alejandro J. Roman, Alexander Hüther, Mariejel L. Weber, Rebecca Kim, Alexander J. Brucker, Artur V. Cideciyan, Tomas S. Aleman

Institutions: University of Pennsylvania, Children's Hospital of Philadelphia

Language: English

Topic: Retinal Development and Disorders

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funder: Research to Prevent Blindness

OpenAlex ID: W7204437183

FWCI: 1.933

Cites: 51

Cited by: 1

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