Application of CRISPR Tools for Variant Interpretation and Disease Modeling in Inherited Retinal Dystrophies

Inherited retinal dystrophies are an assorted group of rare diseases that collectively account for the major cause of visual impairment of genetic origin worldwide. Besides clinically, these vision loss disorders present a high genetic and allelic heterogeneity. To date, over 250 genes have been ass...

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Bibliographic Details
Published in:Genes (Basel)
Main Authors: Fuster-García, Carla, García-Bohórquez, Belén, Rodríguez-Muñoz, Ana, Millán, José M., García-García, Gema
Format: Artigo
Language:Inglês
Published: MDPI 2020
Subjects:
Review
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC7290804/
https://ncbi.nlm.nih.gov/pubmed/32349249
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes11050473
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