In vivo genome editing as a potential treatment strategy for inherited retinal dystrophies

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Title
In vivo genome editing as a potential treatment strategy for inherited retinal dystrophies
Authors
Keywords
Genome editing, In vivo, Retina, CRISPR-Cas, TALEN, AAV, Endonucleases, NHEJ, HDR, MMEJ
Journal
PROGRESS IN RETINAL AND EYE RESEARCH
Volume 56, Issue -, Pages 1-18
Publisher
Elsevier BV
Online
2016-09-13
DOI
10.1016/j.preteyeres.2016.09.001

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