CLINICAL_TRIALS
ClinicalTrials.gov record update
Development of the Tool " iPSC " (Induced Pluripotent Stem Cells) for the Functional Study of Mutations Responsible for Mental Retardation - Application to Familial Study of MYT1L Gene Mutations
This page presents selected fields from the linked source record. It does not add a medical interpretation.
Record identity and dates
- Source
- ClinicalTrials.gov
- Source record ID
- NCT02980302
- Title field or adapter rule
- protocolSection.identificationModule.officialTitle
- Ingested At
- 2026-04-28T10:37:07.655106+00:00
- Published At
- 2018-10-12T00:00:00+00:00
- Record Updated At
- 2018-10-12
- Timestamp Basis
- source retrieval time was not retained by the feed adapter
- Date limitation
- source retrieval time was not retained by the feed adapter
Fields recorded by this source
- protocolSection.conditionsModule.conditions
["Intellectual Deficiency", "Asymptomatic Carrier of the Mutation of the Gene MYT1L", "Healthy Volunteers"]- protocolSection.statusModule.lastUpdatePostDateStruct.date
"2018-10-12"- protocolSection.identificationModule.nctId
"NCT02980302"- protocolSection.identificationModule.officialTitle
"Development of the Tool \" iPSC \" (Induced Pluripotent Stem Cells) for the Functional Study of Mutations Responsible for Mental Retardation - Application to Familial Study of MYT1L Gene Mutations"- protocolSection.statusModule.overallStatus
"COMPLETED"- protocolSection.designModule.phases
["NA"]- protocolSection.statusModule.resultsFirstPostDateStruct.date
""
Study condition terms
Intervention details are not present in the imported fields for this record. No drug-condition relationship is inferred from co-listing.
This index keeps the source fields it imported; it may not contain the complete original record. Verify wording and context in the linked source.