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Foveal Hypoplasia in CRB1-Related Retinopathies

The CRB1 gene plays a role in retinal development and its maintenance. When disrupted, it gives a range of phenotypes such as early-onset severe retinal dystrophy/Leber congenital amaurosis (EOSRD/LCA), retinitis pigmentosa (RP), cone-rod dystrophy (CORD) and macular dystrophy (MD). Studies in CRB1...

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Detalles Bibliográficos
Autores principales:	Rodriguez-Martinez, Ana Catalina, Higgins, Bethany Elora, Tailor-Hamblin, Vijay, Malka, Samantha, Cheloni, Riccardo, Collins, Alexander Mark, Bladen, John, Henderson, Robert, Moosajee, Mariya
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2023
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10531165/ https://www.ncbi.nlm.nih.gov/pubmed/37762234 http://dx.doi.org/10.3390/ijms241813932

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