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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Limbal Stem Cell Deficiency of Genetic Origin: Genotype-phenotype CorrelationLimbus CorneaeRecruitingNot stated2025-12-03NCT02886611

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Research sitesCityCountryLinked trials
Fondation Ophtalmologique Adolphe de RothschildParisFrance4