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Gene Editing as a Potential Therapeutic Solution for Fuchs Endothelial Corneal Dystrophy

Gene Editing as a Potential Therapeutic Solution for Fuchs Endothelial Corneal Dystrophy This Viewpoint explains the possibility of clustered regularly interspaced short palindromic repeats (CRISPR) gene editing becoming a means of treating Fuchs endothelial corneal dystrophy. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png JAMA Ophthalmology American Medical Association

Gene Editing as a Potential Therapeutic Solution for Fuchs Endothelial Corneal Dystrophy

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References (7)

Publisher
American Medical Association
Copyright
Copyright 2018 American Medical Association. All Rights Reserved.
ISSN
2168-6165
eISSN
2168-6173
DOI
10.1001/jamaophthalmol.2018.2324
Publisher site
See Article on Publisher Site

Abstract

This Viewpoint explains the possibility of clustered regularly interspaced short palindromic repeats (CRISPR) gene editing becoming a means of treating Fuchs endothelial corneal dystrophy.

Journal

JAMA OphthalmologyAmerican Medical Association

Published: Sep 21, 2018

There are no references for this article.