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...
Päätekijä: | Fry, LE |
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Muut tekijät: | MacLaren, R |
Aineistotyyppi: | Opinnäyte |
Kieli: | English |
Julkaistu: |
2021
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Aiheet: |
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