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L. Chkioua

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Open access Aug 2026

Ophthalmological and genetic findings associated with CRB1 dysfunction in autosomal recessive retinitis pigmentosa

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 mutations in CRB1 gene that is encoded by the crumbs homolog 1 (CRB1) protein. The aim of this study is to identify the mutations in Alg...

L. Chkioua, Roua Ltaifa, Chayma Sahli et al. · 0 citations

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