Article

Ophthalmological and Genetic Findings Associated with CRB1 Dysfunction in Autosomal Recessive Retinitis Pigmentosa

2026-06-22

Abstract excerpt

<title>Abstract</title> <p> <bold>Introduction:</bold> Retinitis pigmentosa (RP) is an inherited disease of the retina. It is characterized by progressive degeneration of the retinal photoreceptor cells. This pathology is due to the mutations in <italic>CRB1</italic> gene that is encoded by the crumbs homolog 1 (CRB1) protein. The study is aimed to identify the mutations in Algerian patients with Retinitis Pi...

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Literature Corpus work: 7cf8ed1e-2a0e-5765-bf6b-60b042e2ec16
DOI: 10.21203/rs.3.rs-9982851/v1

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