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Leber's Congenital Amaurosis

1 clinical trials · Condition

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RecordFirmDate
Study to Evaluate QR-110 in Leber's Congenital Amaurosis (LCA) Due to the c.2991+1655A>G Mutation (p.Cys998X) in the CEP290 Gene (NCT03140969)Laboratoires Thea2017-10-16

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