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Stargardt patient experiences in the first gene-based clinical trial for an inherited retinal condition in South Africa
Stargardt disease is a genetic condition that causes progressive central vision loss, typically beginning in late childhood or early adulthood. This vision loss is due to a build-up of lipofuscin in the macula, a part of the retina responsible for sharp central vision. Stargardt disease follows an a...
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| Language: | English English |
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Department of Pathology
2025
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