Gene Editing as a Potential Therapeutic Solution for Fuchs Endothelial Corneal Dystrophy: The Future Is Clearer
JAMA Ophthalmol
.
2018 Sep 1;136(9):969-970.
doi: 10.1001/jamaophthalmol.2018.2324.
Authors
Angela Y Zhu
1
,
Vinod Jaskula-Ranga
2
,
Albert S Jun
1
Affiliations
1
Wilmer Eye Institute, Johns Hopkins Medical Institutions, Baltimore, Maryland.
2
Hunterian Medicine, Cambridge, Massachusetts.
PMID:
29931030
DOI:
10.1001/jamaophthalmol.2018.2324
No abstract available
MeSH terms
Fuchs' Endothelial Dystrophy / genetics
Fuchs' Endothelial Dystrophy / therapy*
Gene Editing / methods*
Humans
Transcription Factor 4 / genetics
Substances
TCF4 protein, human
Transcription Factor 4