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

Internet

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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