Clinical and genetic investigations of three Moroccan families with retinitis pigmentosa phenotypes

PURPOSE: Progressive inherited retinal dystrophies, characterized by degeneration of rod photoreceptors and then cone photoreceptors, are known as retinitis pigmentosa (RP), for which 89 genes have been identified. Today, only five Moroccan families with RP with a genetic diagnosis have been reporte...

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Detalles Bibliográficos
Autores principales: Bouzidi, Aymane, Charif, Majida, Bouzidi, Adil, Amalou, Ghita, Kandil, Mostafa, Barakat, Abdelhamid, Lenaers, Guy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7883928/
https://www.ncbi.nlm.nih.gov/pubmed/33633436

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7883928/
https://www.ncbi.nlm.nih.gov/pubmed/33633436

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