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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Precision Diagnosis and Therapy for Rare Diseases by Interpreting Non-coding GenomesCongenital, Hereditary, and Neonatal Diseases and Abnormalities, eye disorder, hereditary disease, nervous system disorder, neuromuscular diseaseRecruitingNot stated2025-01-15NCT06775561

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Research sitesCityCountryLinked trials
IRCCS Azienda Ospedaliero-Universitaria di BolognaBolognaItaly81