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CRISPR to the Rescue: Advances in Gene Editing for the FMR1 Gene

Gene-editing using Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) is promising as a potential therapeutic strategy for many genetic disorders. CRISPR-based therapies are already being assessed in clinical trials, and evaluation of this technology in Fragile X syndrome has been pe...

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Detalles Bibliográficos
Autores principales: Yrigollen, Carolyn M., Davidson, Beverly L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6357057/
https://www.ncbi.nlm.nih.gov/pubmed/30669625
http://dx.doi.org/10.3390/brainsci9010017