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HG004(RPE65-IRDs)LCA is the most common cause of inherited blindness in childhood and constitutes more than 5% of all retinal dystrophies.
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HG301(RHO-adRP)Aims to address RHO-adRP with a single course of treatment
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HG202(nAMD)Characterized by the growth of pathologic choroidal neovascularization (CNV) beneath the macula
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HG204(MDS)The candidate therapeutic, HG204, is developed using HuidaGene's proprietary gene editor delivered by AAV
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HG302(DMD)Duchenne muscular dystrophy (DMD) is a rare, fatal neuromuscular genetic disease and inherited in an X-linked recessive pattern, although de novo germline mutations occur in one-third of patients.