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CRISPR-cas gene-editing as plausible treatment of neuromuscular and nucleotide-repeat-expansion diseases: A systematic review

INTRODUCTION: The system of clustered regularly interspaced short palindromic repeats (CRISPR) and CRISPR-associated proteins (cas) is a new technology that allows easier manipulation of the genome. Its potential to edit genes opened a new door in treatment development for incurable neurological mon...

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Detalles Bibliográficos
Autores principales: Babačić, Haris, Mehta, Aditi, Merkel, Olivia, Schoser, Benedikt
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6386526/
https://www.ncbi.nlm.nih.gov/pubmed/30794581
http://dx.doi.org/10.1371/journal.pone.0212198