Repair of the TGFBI gene in human corneal keratocytes derived from a granular corneal dystrophy patient via CRISPR/Cas9-induced homology-directed repair

Granular corneal dystrophy (GCD) is an autosomal dominant hereditary disease in which multiple discrete and irregularly shaped granular opacities are deposited in the corneal stroma. GCD is caused by a point mutation in the transforming growth factor-β-induced (TGFBI) gene, located on chromosome 5q3...

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Publicado en:Sci Rep
Autores principales: Taketani, Yukako, Kitamoto, Kohdai, Sakisaka, Toshihiro, Kimakura, Mikiko, Toyono, Tetsuya, Yamagami, Satoru, Amano, Shiro, Kuroda, Masahiko, Moore, Tara, Usui, Tomohiko, Ouchi, Yasuo
Formato: Artigo
Lenguaje:Inglês
Publicado: Nature Publishing Group UK 2017
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Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC5711889/
https://ncbi.nlm.nih.gov/pubmed/29196743
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-017-16308-2
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