USH2A Gene Editing Using the CRISPR System

Usher syndrome (USH) is a rare autosomal recessive disease and the most common inherited form of combined visual and hearing impairment. Up to 13 genes are associated with this disorder, with USH2A being the most prevalent, due partially to the recurrence rate of the c.2299delG mutation. Excluding h...

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Detalles Bibliográficos
Autores principales: Fuster-García, Carla, García-García, Gema, González-Romero, Elisa, Jaijo, Teresa, Sequedo, María D., Ayuso, Carmen, Vázquez-Manrique, Rafael P., Millán, José M., Aller, Elena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2017
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5573797/
https://www.ncbi.nlm.nih.gov/pubmed/28918053
http://dx.doi.org/10.1016/j.omtn.2017.08.003

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5573797/
https://www.ncbi.nlm.nih.gov/pubmed/28918053
http://dx.doi.org/10.1016/j.omtn.2017.08.003

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