# Development of the Tool " iPSC " for the Functional Study of Mutations Responsible for Mental Retardation

> **NCT02980302** · NA · COMPLETED · sponsor: **University Hospital, Grenoble** · enrollment: 4 (actual)

## Conditions studied

- Intellectual Deficiency
- Asymptomatic Carrier of the Mutation of the Gene MYT1L
- Healthy Volunteers

## Interventions

- **PROCEDURE:** Cutaneous biopsy

## Key facts

- **NCT ID:** NCT02980302
- **Lead sponsor:** University Hospital, Grenoble
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2015-09
- **Primary completion:** 2017-06
- **Final completion:** 2017-09
- **Target enrollment:** 4 (ACTUAL)
- **Last updated:** 2018-10-12


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT02980302

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT02980302, "Development of the Tool " iPSC " for the Functional Study of Mutations Responsible for Mental Retardation". Retrieved via AI Analytics 2026-05-29 from https://api.ai-analytics.org/clinical/NCT02980302. Licensed CC0.

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