Work

Results of the multicenter study “Registry of patients with inherited retinal dystrophies caused by confirmed biallelic mutations in the RPE65 and RLBP1 genes in Russia (REGINA)”. Report 1. Molecular genetic characteristics of inherited retinal pathologies

Year: 2026

Type: article

Study design: Observational Study

Source: Russian Annals of Ophthalmology

DOI: 10.17116/oftalma202614201170

Authors: V.V. Kadyshev, A.A. Stepanova, K.K. Shefer, I.V. Kondrashina, O.A. Shchagina

Institutions: Research Centre for Medical Genetics, Intersectoral Research and Technology Complex Eye Microsurgery, Novartis (United States)

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

OpenAlex ID: W7139060691

FWCI: 1.939

Cites: 25

Cited by: 1

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