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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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Mol Vis
Päätekijät: Bouzidi, Aymane, Charif, Majida, Bouzidi, Adil, Amalou, Ghita, Kandil, Mostafa, Barakat, Abdelhamid, Lenaers, Guy
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Molecular Vision 2021
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC7883928/
https://ncbi.nlm.nih.gov/pubmed/33633436
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