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Posted: 2025-04-16 23:54:42 UTC
This article contains some claims that remain unverified. While much of the content may be accurate, exercise care when relying on this information.
This article contains some claims that remain unverified. While much of the content may be accurate, exercise care when relying on this information.
Status
Last Updated
2025-04-16 23:55:13 UTC
Verified By
Rollup News
Gene therapy significantly improves vision in infants with severe retinal dystrophy by replacing defective AIPL1 genes, offering hope for addressing genetic blindness in children.
Gene therapy success in treating retinal dystrophy
Replacement of defective AIPL1 genes
Improved vision in infants
Potential for addressing genetic blindness
Severe retinal dystrophy
Defective AIPL1 genes
Genetic blindness