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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...
Tallennettuna:
| Julkaisussa: | Mol Vis |
|---|---|
| Päätekijät: | , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Molecular Vision
2021
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7883928/ https://ncbi.nlm.nih.gov/pubmed/33633436 |
| Tagit: |
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