Development of CRISPR gene therapy for retinal degenerations
<p>Inherited retinal degenerations (IRDs) are a leading cause of blindness, caused by mutations in genes leading to dysfunction and death of cells in the outer retina. Gene-supplementation therapies using adeno-associated viral (AAV) vectors have been developed, however, they are limited to th...
Κύριος συγγραφέας: | Fry, LE |
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Άλλοι συγγραφείς: | MacLaren, R |
Μορφή: | Thesis |
Γλώσσα: | English |
Έκδοση: |
2021
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Θέματα: |
Παρόμοια τεκμήρια
Παρόμοια τεκμήρια
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Developing gene therapy for inherited retinal degenerations
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Multiplexed CRISPR/Cas9 Targeting of Genes Implicated in Retinal Regeneration and Degeneration
ανά: Arife Unal Eroglu, κ.ά.
Έκδοση: (2018-08-01)