| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 4002520 | American Journal of Ophthalmology | 2014 | 15 Pages |
Abstract
Because of a relatively well preserved retinal function, autosomal recessive bestrophinopathy may be a suitable first candidate, among the BEST1-related ocular conditions, for gene replacement therapy.
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Authors
Dror Sharon, Sermed Al-Hamdani, Karl Engelsberg, Liliana Mizrahi-Meissonnier, Alexey Obolensky, Eyal Banin, Birgit Sander, Hanne Jensen, Michael Larsen, Patrik Schatz,