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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

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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

  • Intellectual Deficiency (protocolSection.conditionsModule.conditions)
  • Asymptomatic Carrier of the Mutation of the Gene MYT1L (protocolSection.conditionsModule.conditions)
  • Healthy Volunteers (protocolSection.conditionsModule.conditions)

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