Foveal Hypoplasia in <i>CRB1</i>-Related Retinopathies

Foveal Hypoplasia in <i>CRB1</i>-Related Retinopathies

The <i>CRB1</i> 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...

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Bibliographic Details
Main Authors: Ana Catalina Rodriguez-Martinez, Bethany Elora Higgins, Vijay Tailor-Hamblin, Samantha Malka, Riccardo Cheloni, Alexander Mark Collins, John Bladen, Robert Henderson, Mariya Moosajee
Format: Article
Language:English
Published: MDPI AG 2023-09-01
Series:International Journal of Molecular Sciences
Subjects:
retinal dystrophy
LCA
early-onset severe retinal dystrophy
retinitis pigmentosa (RP)
macular dystrophy (MD)
cone-rod dystrophy (CORD)
Online Access:https://www.mdpi.com/1422-0067/24/18/13932

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https://www.mdpi.com/1422-0067/24/18/13932

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