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Harnessing AAV2-REP1 for Choroideremia Extending Vision in Genetic Retinal Disease

Choroideremia is a rare, inherited retinal disorder that affects countless individuals around the world. Characterized by progressive vision loss, this X-linked condition often starts...

Gene Therapy Using Luxturna How This Revolutionary Treatment Offers New Hope...

Leber’s Congenital Amaurosis (LCA) is a rare genetic disorder that impairs vision from birth or early childhood. Affecting the retina, LCA arises from mutations...

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