Genome Editing in Patient iPSCs Corrects the Most Prevalent USH2A Mutations and Reveals Intriguing Mutant mRNA Expression Profiles

Inherited retinal dystrophies (IRDs) are characterized by progressive photoreceptor degeneration and vision loss. Usher syndrome (USH) is a syndromic IRD characterized by retinitis pigmentosa (RP) and hearing loss. USH is clinically and genetically heterogeneous, and the most prevalent causative gen...

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Detalles Bibliográficos
Autores principales: Sanjurjo-Soriano, Carla, Erkilic, Nejla, Baux, David, Mamaeva, Daria, Hamel, Christian P., Meunier, Isabelle, Roux, Anne-Françoise, Kalatzis, Vasiliki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6938853/
https://www.ncbi.nlm.nih.gov/pubmed/31909088
http://dx.doi.org/10.1016/j.omtm.2019.11.016

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6938853/
https://www.ncbi.nlm.nih.gov/pubmed/31909088
http://dx.doi.org/10.1016/j.omtm.2019.11.016

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