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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Detalles Bibliográficos
Autores principales: Fuster-García, Carla, García-Bohórquez, Belén, Rodríguez-Muñoz, Ana, Millán, José M., García-García, Gema
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7290804/
https://www.ncbi.nlm.nih.gov/pubmed/32349249
http://dx.doi.org/10.3390/genes11050473

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7290804/
https://www.ncbi.nlm.nih.gov/pubmed/32349249
http://dx.doi.org/10.3390/genes11050473

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