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Treating cystic fibrosis with mRNA therapy or CRISPR – EurekAlert
The potential for treating cystic fibrosis (CF) using mRNA therapies or CRISPR gene editing is possible regardless of the causative mutation. CF clinical trials…
IMAGE: Field and provides all-inclusive access to the critical pillars of human gene therapy: research, methods, and clinical applications.
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Credit: Mary Ann Liebert, Inc., publishers
New Rochelle, NY, October 8, 2020–The potential for treating cystic fibrosis (CF) using mRNA therapies or CRISPR gene editing is possible regardless of the causative mutation. CF clinical trials showing that a genotype-agnostic gene therapy for CF is possible are reviewed in the peer-reviewed journal…
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