The Potential of CRISPR/Cas9 Gene Editing as a Treatment Strategy for Inherited Diseases

Clustered regularly interspaced short palindromic repeats (CRISPR) is a promising innovative technology for genomic editing that offers scientists the chance to edit DNA structures and change gene function. It has several possible uses consisting of editing inherited deficiencies, treating, and redu...

Descripción completa

Detalles Bibliográficos
Autores principales: Abdelnour, Sameh A., Xie, Long, Hassanin, Abdallah A., Zuo, Erwei, Lu, Yangqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Cell and Developmental Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8715006/
https://www.ncbi.nlm.nih.gov/pubmed/34977000
http://dx.doi.org/10.3389/fcell.2021.699597

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8715006/
https://www.ncbi.nlm.nih.gov/pubmed/34977000
http://dx.doi.org/10.3389/fcell.2021.699597

Ejemplares similares